HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5960Generated: October 23, 2026
Borohydride → 2-Benzoyloxy-4-hydroxymethylcyclobutanol
https://huagongshe.com/en/reaction/5960
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borohydride | HCID 28123 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Benzoyloxy-4-hydroxymethylcyclobutanone | HCID 19794318 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Benzoyloxy-4-hydroxymethylcyclobutanol | HCID 19794289 | 101.8% |
Reaction Steps
Glacial acetic acid in (25 mL) a 250 mL 3-neck flask was cooled in an ice bath under a stream of nitrogen. Sodium borohydride was added cautiously in portions over a 5 minute period. The ice bath removed and the reagent was used after stirring for 15 minutes at ambient temperature. 2-Benzoyloxy-4-hydroxymethylcyclobutanone (1.43 g, 6.5 mmol) from Step H was dissolved in 45 mL of glacial actetic acid and immediately treated with the above borohydride reagent. After stirring the reaction mixture for 35 minutes, the reaction was quenched with ~2 mL of methanol and the reaction mixture was concentrated in vacuo to a syrup. The syrup was dissolved in 250 mL of ethyl acetate and the ethyl acetate solution was washed with water and 5% aqueous sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated to give 1.47 g of the title compound which was taken on to the next step without purification; MS DCI-NH3M/Z: 221 (M+H)+, 238 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05246931 |
|---|
| Source dataset | uspto-grants-1993_09 |
|---|
| ORD ID | ord-c6befcbde27c4bafadace118dde28422 |
|---|
| Source note | uspto-grants-1993_09 |
|---|