HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 2-Difluoromethoxy-alpha-cyano-benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 2-(Difluoromethoxy)benzaldehyde | HCID 2736984 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Difluoromethoxy-alpha-cyano-benzyl alcohol | HCID 43436629 | — |
Reaction Steps
7.2 g of potassium cyanide were dissolved in 30 ml of water and 6 ml of ethanol, while cooling. 16 g of 2-difluoromethoxybenzaldehyde were then added at 0°-5° C., while cooling. After subsequently stirring the mixture between 0° and 10° C. for 20 minutes, a mixture of 7 ml of concentrated H2SO4 and 18 ml of water was added dropwise. The mixture was subsequently stirred for a further 2 hours and was thereby allowed to come to room temperature. After extracting twice with methylene chloride, the organic phase was dried and the solvent was distilled off. 2-Difluoromethoxy-α-cyano-benzyl alcohol was obtained as a colorless oil, the structure of which was confirmed by a nuclear magnetic resonance spectrum. The yield was virtually quantitative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04596880 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-f4ef9fef6a17434f899741f4397a4cce |
| Source note | uspto-grants-1986_06 |