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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591035Generated: October 30, 2026

Water → HCID 70855554, compound

https://huagongshe.com/reaction/591035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 70855553HCID 70855553—
ReactantSodium tetraborohydrideHCID 131720822—
SolventEthyl AcetateHCID 8857—
SolventThionyl ChlorideHCID 24386—
ProductHCID 70855554HCID 70855554—

Reaction Steps

A solution of 3-bromo-4-methyl-benzo[b]thiophene-2-carboxylic acid (23c) (420 mg, 1.55 mmol) in thionyl chloride (10 mL) was refluxed for 1 hour. Thionyl chloride was then evaporated under reduced pressure and the residue was diluted with dimethoxyethane (20 mL). Sodium tetraborohydride (70 mg, 1.85 mmol) was then added to the solution. After 1 hour, the mixture was hydrolyzed with water (5 mL) and diluted with ethyl acetate (20 mL). The organic layer was washed with brine (10 mL), dried over sodium sulfate, filtered and evaporated to dryness to afford the desired alcohol (23d) as a white solid without further purification (400 mg, 1.55 mmol, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-4d3f119bc0c44eb9aa475daca1429abf
Source noteuspto-grants-2016_01