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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058336Generated: November 1, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → Tert-butyl 2-(aminomethyl)-4-chlorobenzylcarbamate

https://huagongshe.com/reaction/1058336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantTert-butyl 4-chloro-2-(hydroxymethyl)benzylcarbamateHCID 12052444—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 2-(aminomethyl)-4-chlorobenzylcarbamateHCID 11149921—

Reaction Steps

To a solution of tert-butyl 4-chloro-2-(hydroxymethyl)benzylcarbamate (10 g, 36.8 mmol) in anhydrous THF (100 ml) was added DPPA (8.3 ml, 38.6 mmol) and DBU (5.79 ml, 38.6 mmol). The mixture was stirred overnight and then was partitioned between ethyl acetate and water. The organic layer was washed with brine, and was concentrated in vacuo to a crude oil (14.6 g). Purification was accomplished by silica gel chromatography, eluting a gradient of ethyl acetate-hexane (10, 15, 20, 25, 50%) to give tert-butyl 2-(aminomethyl)-4-chlorobenzylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515011B2
Source datasetuspto-grants-2003_02
ORD IDord-966e639c23184c068a0a97eee6f3ce12
Source noteuspto-grants-2003_02