HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34606Generated: October 29, 2026
Acetic Acid → 3-Benzyl-4-fluorobenzaldehyde
https://huagongshe.com/reaction/34606
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 3-Benzyl-4-fluorobenzaldehyde | HCID 13854280 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Benzyl-4-fluorobenzaldehyde | HCID 13854280 | — |
| Product | alpha-Cyano-3-benzyl-4-fluorobenzyl alcohol | HCID 13911474 | — |
Reaction Steps
A solution of potassium cyanide (0.26 g) in water (2 cm3) was added portionwise to a suspension of 3-benzyl-4-fluorobenzaldehyde (0.5 g) in glacial acid (10 cm3) whilst the temperature was maintained at 0° C. After 30 minutes, the reaction mixture was allowed to warm to the ambient temperature (ca. 25° C.), and allowed to stand for a period of 16 hours. A further portion of glacial acetic acid (5 cm3) was added and stirring continued for 8 hours at the ambient temperature. After standing for sixteen hours, a further portion of potassium cyanide (0.26 g) in water (1 cm3) was added, and after the reaction mixture had been allowed to stand for a period of 7 days, it was diluted with water, and extracted with diethyl ether. The ethereal layer was washed sequentially with aqueous sodium bicarbonate, and brine, dried, and the solvent evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel using hexane containing diethyl ether (40% by volume) as eluent to give firstly recovered 3-benzyl-4-fluorobenzaldehyde (0.2 g), and secondly α-cyano-3-benzyl-4-fluorobenzyl alcohol (0.24 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04762835 |
|---|
| Source dataset | uspto-grants-1988_08 |
|---|
| ORD ID | ord-e6f169fadf73490d8ee2b4aa302af80b |
|---|
| Source note | uspto-grants-1988_08 |
|---|