Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620633Generated: October 27, 2026

Water → Ethyl 1-[2,4-bis(trifluoromethyl)benzyl]-7-oxoazepane-4-carboxylate

https://huagongshe.com/reaction/1620633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2,4-Bis(trifluoromethyl)benzyl bromideHCID 518871—
ReactantEthyl 7-oxoazepane-4-carboxylateHCID 23093698—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 1-[2,4-bis(trifluoromethyl)benzyl]-7-oxoazepane-4-carboxylateHCID 8667880068.6%

Reaction Steps

To a solution of ethyl 7-oxoazepane-4-carboxylate (9.78 g) in THF (250 mL) was added 60% sodium hydride (2.33 g, containing mineral oil) under ice-cooling. The reaction mixture was stirred for 5 min under ice-cooling, and 1-(bromomethyl)-2,4-bis(trifluoromethyl)benzene (17.9 g) was added. The reaction mixture was stirred at room temperature overnight, water was added, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/petroleum ether) to give the title compound (14.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-d8b1d17594cd4951af388d45bcd432dd
Source noteuspto-grants-2014_07