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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838762Generated: November 1, 2026

Triethylamine → HCID 22229205, compound

https://huagongshe.com/reaction/1838762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantBenzyl piperazine-1-carboxylateHCID 643495—
Reactanttert-butyl N-{[4-(aminomethyl)phenyl]methyl}carbamateHCID 3354775—
SolventDichloromethaneHCID 6344—
ProductHCID 22229205HCID 2222920581.5%

Reaction Steps

At 0° C., 25.0 g (106 mmol) of 4-(tert-butyloxycarbonylaminomethyl)benzylamine in 150 ml of dichloromethane are added dropwise to a solution of 22.4 g (111 mmol) of 4-nitrophenyl chloroformate in 200 ml of dichloromethane, and the mixture is stirred for 10 min. 15.6 ml (111 mmol) of triethylamine are then added dropwise, and the mixture is stirred at RT for 1.5 h. At 0° C., initially 24.5 g (111 mmol) of benzyl piperazine-1-carboxylate in 80 ml of dichloromethane and then 15.6 ml (111 mmol) of triethylamine are added dropwise. The mixture is stirred at RT for 16 h. The solvent is removed from the reaction mixture and the crude product is chromatographed over silica gel (toluene/ethyl acetate=1:1). Crystallization from diisopropyl ether gives 41.7 g of the title compound as a colorless solid of m.p. 108-112° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673786B1
Source datasetuspto-grants-2004_01
ORD IDord-4bd2ce9341b04b629a38aae1bd9fe8b3
Source noteuspto-grants-2004_01