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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252206Generated: November 1, 2026

Sodium borohydride → HCID 57108405, compound

https://huagongshe.com/reaction/1252206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57097043HCID 57097043—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 57108405HCID 57108405—

Reaction Steps

A mixture of sodium borohydride (38 mg) and 1-(di-p-anisylmethyl)-3-acetyl-4-acetoxy-2-azetidinone (397 mg) in isopropanol (6 ml) was stirred for 0.5 hour at room temperature. The reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and evaporated to give 1-(di-p-anisylmethyl)-3-(1-hydroxyethyl)-4-acetoxy-2-azetidinone (the product was a mixture of two stereoisomers (about 1:1) of hydroxyethyl group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742052
Source datasetuspto-grants-1988_05
ORD IDord-bf6e5099b9954d57b899102579e77b78
Source noteuspto-grants-1988_05