SU249396A1 - Method of producing 1-naphthol-3,6-disulfonic acid - Google Patents

Method of producing 1-naphthol-3,6-disulfonic acid

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Publication number
SU249396A1
SU249396A1 SU1177267A SU1177267A SU249396A1 SU 249396 A1 SU249396 A1 SU 249396A1 SU 1177267 A SU1177267 A SU 1177267A SU 1177267 A SU1177267 A SU 1177267A SU 249396 A1 SU249396 A1 SU 249396A1
Authority
SU
USSR - Soviet Union
Prior art keywords
naphthol
disulfonic acid
producing
acid
yield
Prior art date
Application number
SU1177267A
Other languages
Russian (ru)
Original Assignee
Н. Н. Лемин
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Н. Н. Лемин filed Critical Н. Н. Лемин
Priority to SU1177267A priority Critical patent/SU249396A1/en
Application granted granted Critical
Publication of SU249396A1 publication Critical patent/SU249396A1/en

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Description

1-Нафтол-3,6-дисульфокислота примен етс  как азососта1вл гон1,а  в производстве азокрасителей и активных красителей.1-Naphthol-3,6-disulfonic acid is used as azo-aostavol gon1, and in the manufacture of azo dyes and active dyes.

Известен способ получени  1-нафтол-3,6-дисульфокислоты из нафталин-1,3,6-трисульфокислоты щелочным плавлением под давлением . Выход 50-52%.A known method for producing 1-naphthol-3,6-disulfonic acid from naphthalene-1,3,6-trisulfonic acid by alkali fusion under pressure. Yield 50-52%.

С целью повышени  выхода целевого продукта предлагаетс  Ьпафтол-З.б-дисульфокислоту получать кип чением щелочного раствора 1-иафтол-3,6,8-трисульфокислоты с цинковой пылью в присутствии небольшой добавки хлористого олова с последующим выделением целевого продукта известными методами . Выход продукта в растворе 98-99%, в сухом виде 88-89% от теории. Степень превращени  1-нафтол-3,6,8-трисульфокислоты в целевой продукт устанавливают хроматографически , а также определ ют сульфит натри , образующийс  при отщеплении сульфогруппы в 1 -нафтол-3,6,8-трисульфокислоте.In order to increase the yield of the target product, β-naphthol-Z.b-disulfonic acid is proposed to be obtained by boiling an alkaline solution of 1-yaftol-3,6,8-trisulfonic acid with zinc dust in the presence of a small addition of tin chloride, followed by isolation of the target product by known methods. The product yield in solution 98-99%, in dry form 88-89% of theory. The degree of conversion of 1-naphthol-3,6,8-trisulfonic acid to the target product is established by chromatography, and sodium sulfite, which is formed upon cleavage of the sulfo group in 1-naphthol-3,6,8-trisulfonic acid, is also determined.

Пример. 16,47 г (0,03 г-моль) 70%-ной 1нафтол-3 ,6,8-трисульфокислоты перемешиваютExample. 16.47 g (0.03 g-mol) of 70% 1-naphthol-3, 6,8-trisulfonic acid are mixed

при 113-114°С в течение 30 час в 30 мл 25%-ного водного раствора едкого натра с 4,5 г цинковой пыли и 0,15 г хлористого олова . После фильтрации и промывки цинковогоat 113-114 ° C for 30 hours in 30 ml of a 25% aqueous solution of caustic soda with 4.5 g of zinc dust and 0.15 g of tin chloride. After filtration and rinsing zinc

шлама получают 200 лы щелочного раствора, содержащего 8,97 г 100%-ной 1-нафтол-3,6-дисульфокислоты . Выход 98,24%. Щелочной раствор нейтрализуют сол ной кислотой до рН 8,0, отфильтровывают и промывают выпа-вшийsludge is obtained 200 ly of an alkaline solution containing 8.97 g of 100% 1-naphthol-3,6-disulfonic acid. Yield 98.24%. The alkaline solution is neutralized with hydrochloric acid to pH 8.0, filtered and the precipitate washed.

осадок. Затем упаривают до 60 мл и высаливают 6 г поваренной соли. После выдержки выпавший осадок фильтруют и сушат при 85- 90°С. Получают 16,51 г 49,2%-ной 1-нафтол3 ,6-дисульфокислоты. Выход 89% от теории.sediment. Then it is evaporated to 60 ml and 6 g of salt are salted out. After aging, the precipitated precipitate is filtered and dried at 85-90 ° C. 16.51 g of 49.2% 1-naphthol 3, 6-disulfonic acid are obtained. Output 89% of theory.

Предмет изобретени Subject invention

Способ получени  1-нафтол-3,6-дисульфокислоты , отличающийс  тем, что, с целью повышени  выхода целевого продукта, щелочной раствор 1-нафтол-3,6,8-трисульфокислоты кип т т с цинковой цылью в присутствии хлористого олова с последующим выделением целевого продукта известным способом.The method of producing 1-naphthol-3,6-disulfonic acid, characterized in that, in order to increase the yield of the target product, an alkaline solution of 1-naphthol-3,6,8-trisulfonic acid is boiled with zinc dust in the presence of tin chloride, followed by separation target product in a known manner.

SU1177267A 1967-08-03 1967-08-03 Method of producing 1-naphthol-3,6-disulfonic acid SU249396A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU1177267A SU249396A1 (en) 1967-08-03 1967-08-03 Method of producing 1-naphthol-3,6-disulfonic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU1177267A SU249396A1 (en) 1967-08-03 1967-08-03 Method of producing 1-naphthol-3,6-disulfonic acid

Publications (1)

Publication Number Publication Date
SU249396A1 true SU249396A1 (en) 1973-10-03

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105777590A (en) * 2014-12-26 2016-07-20 沈阳化工研究院有限公司 Preparation method of dye intermediate 1-naphthol-3,6-disulfonic acid (RG acid)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105777590A (en) * 2014-12-26 2016-07-20 沈阳化工研究院有限公司 Preparation method of dye intermediate 1-naphthol-3,6-disulfonic acid (RG acid)
CN105777590B (en) * 2014-12-26 2017-09-15 沈阳化工研究院有限公司 A kind of preparation method of the disulfonic acid of 1 naphthols of dyestuff intermediate 3,6 (RG acid)

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