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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241379Generated: October 30, 2026

Benzyl Bromide → HCID 86652870, compound

https://huagongshe.com/reaction/241379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86652871HCID 86652871—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86652870HCID 8665287024%

Reaction Steps

To an ice-cold solution of ethyl 4-[1-hydroxyimino-3-[3-isopropyl-6-(trifluoromethyl)benzothiophen-2-yl]propyl]-2-methylphenoxyacetate [Example 16 (1)] (90 mg, 0.18 mmol) in THF (1.8 mL) was added 55% sodium hydride (12 mg, 0.27 mmol). The mixture was stirred for 10 minutes, to which was added benzyl bromide (0.03 mL, 0.3 mmol). The mixture was stirred for 72 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 colorless oil (25 mg, yield 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648208B2
Source datasetuspto-grants-2014_02
ORD IDord-22558c2cc94347a7a320a2553aff2be6
Source noteuspto-grants-2014_02