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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785224Generated: October 29, 2026

Sodium borohydride → [3-Isopropenyl-5-(4-trifluoromethyl-phenyl)-thiophen-2-yl]-methanol

https://huagongshe.com/reaction/1785224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86604774HCID 86604774—
SolventTetrahydrofuranHCID 8028—
Product[3-Isopropenyl-5-(4-trifluoromethyl-phenyl)-thiophen-2-yl]-methanolHCID 68853480—

Reaction Steps

To a solution of 3-Isopropenyl-5-(4-trifluoromethyl-phenyl)-thiophene-2-carbaldehyde (0.084 g, 0.283 mmole) in THF (3 mL), is added to NaBH4 (0.023 g, 0.622 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 saturated NH4Cl(aq) (20 mL) at 0° C. The THF is removed on rota vapor, the aqueous solution is then extracted with ethyl acetate (2×10 mL). The combined organic solution is washed with brine (3×20 mL), dried over Na2SO4 and concentrated to provide the titled compound as yellow solid, which is used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504433B2
Source datasetuspto-grants-2009_03
ORD IDord-e70bee66491d4194abaaf67ed0f9b594
Source noteuspto-grants-2009_03