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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068434Generated: October 30, 2026

1-(Bromomethyl)-3-(trifluoromethoxy)benzene → HCID 54425085, compound

https://huagongshe.com/reaction/1068434

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)-3-(trifluoromethoxy)benzeneHCID 737176—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant1-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylateHCID 2758812—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54425085HCID 54425085—

Reaction Steps

To a cold (−78° C.) solution of ethyl N-tert-butoxycarbonylpiperidine-4-carboxylate (5.16 g, 20.05 mmol) in anhydrous tetrahydrofuran (60 mL), a solution of sodium bis(trimethylsilyl)amide (28 mL, 1M, 28 mmol) was added over a period of 30 min. The resultant mixture was stirred at −78° C. for 1 h, and 3-(trifluoromethoxy)benzyl bromide (5.90 g, 23.14 mmol) was added. The reacting mixture was allowed to warm to room temp. and stirred overnight. The product mixture was concentrated, and the residue was partitioned between water and ethyl acetate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with 20% ethyl acetate in hexane. Collection and concentration of appropriate fractions provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248756B1
Source datasetuspto-grants-2001_06
ORD IDord-e63540c3adaf4927bca38732387e2492
Source noteuspto-grants-2001_06