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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785217Generated: October 25, 2026

Lithium borohydride → 2-Thiophenemethanol, 5-[4-(trifluoromethyl)phenyl]-

https://huagongshe.com/reaction/1785217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
Reactant5-(4-(Trifluoromethyl)phenyl)thiophene-2-carbaldehydeHCID 4674819—
SolventTetrahydrofuranHCID 8028—
Product2-Thiophenemethanol, 5-[4-(trifluoromethyl)phenyl]-HCID 21986352—

Reaction Steps

To a solution of 5-(4-Trifluoromethyl-phenyl)-thiophene-2-carbaldehyde (3.02 g, 11.8 mmole) in THF (100 mL), is added to LiBH4 (1.75 g, 80.24 mmole) in one portion at 0° C. The reaction is kept at 0° C. for 15 minutes and warmed up to room temperature for 1 hour. The reaction is quenched using 5N HCl (100 mL) at 0° C. The THF is removed on rota vapor, the aqueous solution is then extracted with ethyl acetate (2×100 mL). The combined organic solution is washed with brine (3×200 mL), dried over Na2SO4 and concentrated. The crude product is purified on a silica gel column, eluting with 20% ethyl acetate in hexane and concentrated to provide the titled compound as off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504433B2
Source datasetuspto-grants-2009_03
ORD IDord-d9b5e75adf0e48869f9a9fff941b564e
Source noteuspto-grants-2009_03