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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307532Generated: November 1, 2026

Sodium borohydride → HCID 69946895, compound

https://huagongshe.com/reaction/2307532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 69740094HCID 69740094—
SolventMethanolHCID 887—
ProductHCID 69946895HCID 6994689550%

Reaction Steps

Sodium borohydride (27 mg, 0.708 mmol) was added to a magnetically stirred solution of trans-2-carboethoxy-5-acetoxy-1,3-oxathiolane (52 mg, 0.236 mmol) in methanol (1 mL) at 0° C. under an argon atmosphere. The resultant solution was stirred for 25 minutes at 0° C. The reaction was quenched with 2 drops of saturated ammonium chloride solution followed by dilution with diethyl ether (4 mL). This mixture was stirred at room temperature for 15 minutes and then was dried over anhydrous magnesium sulphate. The drying agent was removed by suction filtration and the filtrate was concentrated under reduced pressure. The crude product obtained was subjected to column chromatography (50% EtOAc-hexane) to afford 21 mg (50%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831174B2
Source datasetuspto-grants-2004_12
ORD IDord-089d0fd374ad4b49812733a704237a35
Source noteuspto-grants-2004_12