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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241378Generated: November 3, 2026

Benzyl chloroformate → Benzyl 1-(4-fluorophenyl)-2-oxoazepane-3-carboxylate

https://huagongshe.com/reaction/2241378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-(4-Fluorophenyl)azepan-2-oneHCID 67515800—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 1-(4-fluorophenyl)-2-oxoazepane-3-carboxylateHCID 6851702055.3%

Reaction Steps

A solution of 1-(4-fluorophenyl)azepan-2-one (1.1 g, 5.3 mmol) was dissolved in THF (5 mL) and was added into LDA (11 mmol) at −78° C. and stirred for 5 minutes. Benzyl chloroformate (1.6 ml, 11 mmol) was added at −78° C. and the reaction warmed to ambient temperature. The solution was poured into ice and diluted with EtOAc (100 mL). The organic layer washed with brine, dried with Na2SO4, filtered and concentrated. The residue was purified by column chromatography (50% EtOAc in hexane) to afford the product (1 g, 55% yield) as brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723330B2
Source datasetuspto-grants-2010_05
ORD IDord-2f7e45f320bc45df8583e7697861fcb5
Source noteuspto-grants-2010_05