GB874774A - Carbamates of 5,5-bis-hydroxymethyl-1,3-dioxan substituted in the 2-position - Google Patents
Carbamates of 5,5-bis-hydroxymethyl-1,3-dioxan substituted in the 2-positionInfo
- Publication number
- GB874774A GB874774A GB12084/60A GB1208460A GB874774A GB 874774 A GB874774 A GB 874774A GB 12084/60 A GB12084/60 A GB 12084/60A GB 1208460 A GB1208460 A GB 1208460A GB 874774 A GB874774 A GB 874774A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrogen
- alkyl
- acid
- radical
- aryl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises carbamates of the formula <FORM:0874774/IV (b)/1> (wherein R1 is hydrogen or an alkyl radical, R2 is an alkyl, halogenated alkyl, alkenyl or aryl radical, R3 is hydrogen, an alkyl radical of at most 3 carbon atoms or an aryl or alkaryl radical, R4 is hydrogen or an alkyl radical of at most 3 carbon atoms and X is hydrogen or the group -CONR5R6 wherein R5 and R6 correspond to the definitions given for R3 and R4 respectively) and their preparation by reacting a compound of the formula <FORM:0874774/IV (b)/2> with (a) a reactive functional derivative of the appropriate carbamic acid R3R4NCOOH; or (b) a reactive derivative of carbonic acid and then treating the intermediate product with the appropriate amine NHR3R4; or (c) cyanic acid or an isocyanate R3NCO. Suitable derivatives for use in (a) and (b) include carbamyl chlorides R3R4NCOCl, carbamic acid esters, phosgene and aliphatic or aromatic chloroformates, while (c) is preferably effected either with the use of cyanic acid obtained in situ by reacting an alkali metal cyanate with a strong organic acid or by heating cyanuric acid or urea or with the use of a lower alkyl or aryl isocyanate. Examples are given. Diols of the second general formula above are prepared from pentaerythritol and the appropriate aldehydes or ketones.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH874774X | 1959-04-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB874774A true GB874774A (en) | 1961-08-10 |
Family
ID=4544312
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12084/60A Expired GB874774A (en) | 1959-04-10 | 1960-04-05 | Carbamates of 5,5-bis-hydroxymethyl-1,3-dioxan substituted in the 2-position |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB874774A (en) |
-
1960
- 1960-04-05 GB GB12084/60A patent/GB874774A/en not_active Expired
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