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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5960Generated: October 23, 2026

Borohydride → 2-Benzoyloxy-4-hydroxymethylcyclobutanol

https://huagongshe.com/en/reaction/5960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorohydrideHCID 28123—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Benzoyloxy-4-hydroxymethylcyclobutanoneHCID 19794318—
SolventAcetic AcidHCID 176—
Product2-Benzoyloxy-4-hydroxymethylcyclobutanolHCID 19794289101.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246931
Source datasetuspto-grants-1993_09
ORD IDord-c6befcbde27c4bafadace118dde28422
Source noteuspto-grants-1993_09