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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785237Generated: October 30, 2026

Sodium borohydride → HCID 57594981, compound

https://huagongshe.com/reaction/1785237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57594990HCID 57594990—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57594981HCID 57594981—

Reaction Steps

To a solution of 2-[3-Methyl-5-(4-trifluoromethyl-phenyl)-thiophen-2-yl]-propionaldehyde (1.40 g, 4.69 mmole) in THF (20 mL), is added to NaBH4 (0.266 g, 7.04 mmole) in one portion at 0° C. The reaction is kept at 0° C. for 15 minutes and warmed up to room temperature for 2 hours. The reaction is quenched using NH4Cl(aq) (50 mL) at 0° C. The THF is removed on rota vapor, the aqueous solution is then extracted with ethyl acetate (2×50 mL). The combined organic solution is washed with brine (3×100 mL), dried over Na2SO4 and concentrated. The crude product is purified on a silica gel column, gradient eluting with 0-20% ethyl acetate in hexane and concentrated to provide the titled compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504433B2
Source datasetuspto-grants-2009_03
ORD IDord-544a0915018b4af0ad3c53ce5e7a3704
Source noteuspto-grants-2009_03