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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241377Generated: October 26, 2026

Sodium amide → Methyl 3-[4-[1-[2-[3-isopropyl-6-(trifluoromethyl)-benzothiophen-2-yl]ethyl]vinyl]-2-methylphenyl]propionate

https://huagongshe.com/reaction/241377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium amideHCID 24533—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylphosphonium bromideHCID 22062633—
ReactantMethyl 3-[4-[3-[3-isopropyl-6-(trifluoromethyl)benzothiophen-2-yl]propionyl]-2-methylphenyl]propionateHCID 66883002—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-[4-[1-[2-[3-isopropyl-6-(trifluoromethyl)-benzothiophen-2-yl]ethyl]vinyl]-2-methylphenyl]propionateHCID 6688445936%

Reaction Steps

To a suspension of trimethylphosphonium bromide (84 mg, 0.24 mmol) in THF (4 mL) was added sodium amide (12 mg, 0.31 mmol) under N2 atmosphere. The mixture was stirred for 30 minutes at room temperature, to which was added a solution of methyl 3-[4-[3-[3-isopropyl-6-(trifluoromethyl)benzothiophen-2-yl]propionyl]-2-methylphenyl]propionate [Example 12 (7)] (75 mg, 0.16 mmol) in THF (1 mL). The mixture was stirred for 22 hours at room temperature, treated with saturated aqueous ammonium chloride solution, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=7/1), to give the titled compound as a pale yellow oil (27 mg, yield 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648208B2
Source datasetuspto-grants-2014_02
ORD IDord-206b1abdfa8c40adbd096a311bc4b394
Source noteuspto-grants-2014_02