HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Cyanophenylethyl cyclopropyl carbinol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13316970 | HCID 13316970 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Cyanophenylethyl cyclopropyl carbinol | HCID 13316971 | 99.3% |
Reaction Steps
To a solution of 30.9 g of 4-cyanophenylethyl cyclopropyl ketone in 90 ml of absolute ethanol was added 1.48 g of sodium borohydride, and the mixture was stirred at room temperature for three hours. The product isolated from the reaction still contained unreacted starting material, so the material was redissolved in 90 ml of ethanol and treated with 0.7 g additional sodium borohydride for three hours. The product obtained by evaporation of the solvent, trituration of the residue with methylene dichloride and water, and isolation of the product from the organic phase, gave 31.0 g of 4-cyanophenylethyl cyclopropyl carbinol as an oil which crystallized to a colorless solid, m.p. 70°-71° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04451476 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-675197aaecaa49c4a4d2dca8a72e0cd7 |
| Source note | uspto-grants-1984_05 |