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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785229Generated: October 31, 2026

3-Acetyl-2-methyl-5-phenylthiophene → HCID 57594999, compound

https://huagongshe.com/reaction/1785229

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Acetyl-2-methyl-5-phenylthiopheneHCID 2728765—
ReactantLithium borohydrideHCID 4148881—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57594999HCID 57594999—

Reaction Steps

To a solution of 1-(2-Methyl-5-phenyl-thiophen-3-yl)-ethanone (1.08 g, 5.00 mmole) in THF (20 mL), is added to LiBH4 (0.327 g, 15.0 mmole) in one portion at 0° C. The reaction is kept at 0° C. for 30 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 (3×50 mL). The combined organic solution is dried over Na2SO4 and concentrated to provide the titled compound as white 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-dfee3024901a41058eca4305c84c80f0
Source noteuspto-grants-2009_03