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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848788Generated: October 31, 2026

Ethanol → Fasiglifam

https://huagongshe.com/reaction/1848788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant[6-({2',6'-Dimethyl-4'-[3-(methylsulfonyl)propoxy]biphenyl-3-yl}methoxy)-1-benzofuran-3-yl]acetic acidHCID 86706791—
SolventTriethylamineHCID 8471—
ProductFasiglifamHCID 2485728699.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

Under an argon atmosphere, to [6-({2′,6′-dimethyl-4′-[3-(methylsulfonyl)propoxy]biphenyl-3-yl}methoxy)-1-benzofuran-3-yl]acetic acid (522 mg), dichloro[(+)-1,2-bis((2R,5R)-2,5-diisopropylphosphorano)benzene]ruthenium (II)-N,N-dimethylformamide complex (7.4 mg) in an autoclave container was added a solution of dehydrated ethanol (6 mL) containing triethylamine (0.139 mL), and the mixture was stirred at 50° C. for 24 hr under a hydrogen atmosphere (1 MPa). The reaction mixture was concentrated, 10% aqueous citric acid solution (25 mL) and ethyl acetate (25 mL) were added, and an extraction operation was performed. The aqueous layer was extracted with ethyl acetate (25 mL), and the combined organic layer was washed with water (25 mL), dried over sodium sulfate and concentrated. The crude product was washed with diisopropyl ether. After filtration, the obtained solid was dried at 50° C. under reduced pressure to give the title compound (523 mg) as white crystals. 80.0% ee.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952185B2
Source datasetuspto-grants-2015_02
ORD IDord-c50cb3cecb53416cb03b2fc816d45bda
Source noteuspto-grants-2015_02