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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080710Generated: October 27, 2026

Sodium borohydride → Methyl thien-2-yl-hydroxyacetate

https://huagongshe.com/reaction/1080710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl alpha-oxo-2-thiopheneacetateHCID 11217486—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductMethyl thien-2-yl-hydroxyacetateHCID 1368235688.4%

Reaction Steps

To a stirred solution of methyl 2-thiopheneglyoxylate (1.01 g) in ethanol (20 ml) in an ice bath was added sodium borohydride (0.113 g) in 1 ml of water, and the mixture was stirred for 10 minutes. The reaction was quenched with aqueous acetic acid and the mixture was partitioned between methylene chloride and water. The organic extract was washed with brine, dried (sodium sulfate) and evaporated to give methyl α-hydroxy-2-thienylacetate as an oil (0.903 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05583147
Source datasetuspto-grants-1996_12
ORD IDord-657ee4f9087f4328a004c25ec7dafb83
Source noteuspto-grants-1996_12