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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500685Generated: October 30, 2026

Sodium borohydride → HCID 57443976, compound

https://huagongshe.com/reaction/500685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57443972HCID 57443972—
SolventTetrahydrofuran ethanolHCID 21873804—
ProductHCID 57443976HCID 57443976—

Reaction Steps

To a cooled (0° C.) solution of ethyl 6-acetyl-1-benzothiophene-2-carboxylate (2.0 g, 8.06 mmol) in THF/EtOH (20/20 mL) was added sodium borohydride (308 mg, 8.14 mmol) portionwise. After 2 h, the reaction was quenched with sat. NH4Cl. The resulting mixture diluted with EtOAc (40 mL), washed with water and brine. The organic layer was dried over Na2SO4, filtered and concentrated. The resultant residue (2.1 g) was used without further purification. MS (EI): cal'd 251 (MH+), exp 251 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772238B2
Source datasetuspto-grants-2010_08
ORD IDord-12774d699f8349848baf8fe73c7b78c3
Source noteuspto-grants-2010_08