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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843958Generated: October 26, 2026

Ethyl Acetate → (5-Fluoro-1-benzothiophen-2-yl)methanol

https://huagongshe.com/reaction/1843958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantMethyl 5-fluoro-1-benzothiophene-2-carboxylateHCID 22473847—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product(5-Fluoro-1-benzothiophen-2-yl)methanolHCID 3699559483.33%

Reaction Conditions

Temperature-10 °C

Reaction Steps

DIBAL-H (59.4 mL, 59.41 mmol) was added to a solution of methyl 5-fluorobenzo[b]thiophene-2-carboxylate (I-50a: 2.5 g, 11.882 mmol) in THF (75 mL) at −70° C. and the resulting reaction mass was stirred at −10° C. for 2 hours. The reaction was monitored by TLC (30% ethyl acetate in hexane). The reaction mass was quenched with methanol at −70° C. and concentrated under reduced pressure. The crude residue obtained was partitioned between water and ethyl acetate. The organic layer was dried over Na2SO4 and concentrated under reduced pressure to afford the crude product. Purification by column chromatography on silica gel (15% ethyl acetate in hexane) afforded 1.8 g of the product (83.33% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946260B2
Source datasetuspto-grants-2015_02
ORD IDord-5f9944555000483286c8ad2335b14e60
Source noteuspto-grants-2015_02