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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851391Generated: October 30, 2026

Sodium borohydride → HCID 13091200, compound

https://huagongshe.com/reaction/851391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57221866HCID 57221866—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 13091200HCID 1309120062.1%

Reaction Steps

(3S,4R)-3-[(1RS)-1-(p-Nitrobenzyloxycarbonyloxy)ethyl]-2-oxo-4-(2-oxoethyl)azetidine (8 mg) was dissolved in methanol (0.8 ml) and sodium borohydride (2 mg) was added at 0° C. The mixture was then stirred for 30 minutes at the same temperature and acetic acid (3 drops) was added. The mixture was evaporated and the residue was dissolved in ethyl acetate, washed with aqueous sodium bicarbonate, and brine, dried over magnesium sulfate and evaporated. The residue was purified by preparative thin layer chromatography (silica gel) developing with benzene: acetone (1:1) to give (3S,4R)-4-(2-hydroxyethyl)-3-[(1RS)-1-(p-nitrobenzyloxycarbonyloxy)ethyl]-2-oxoazetidine (5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04383945
Source datasetuspto-grants-1983_05
ORD IDord-3c01453409fc43ea9bd66f39e77fba04
Source noteuspto-grants-1983_05