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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80985Generated: October 26, 2026

Acetic Acid → tert-Butyl (2-((4-chlorobenzyl)amino)ethyl)carbamate

https://huagongshe.com/reaction/80985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantN-BOC-ethylenediamineHCID 187201—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,1-DichloroethaneHCID 6365—
Producttert-Butyl (2-((4-chlorobenzyl)amino)ethyl)carbamateHCID 6713487790%

Reaction Steps

Sodium triacetoxyborohydride (3.3 g, 15.4 mmol, 1.1 eq.) was added at room temperature to a solution of 4-chlorobenzaldehyde (2 g, 14 mmol), tert-butyl 2-aminoethylcarbamate (4.5 mL, 28.5 mmol, 1.2 eq.) and acetic acid (2.5 mL) in dichloroethane (20 mL). The reaction mixture was allowed to stir overnight before being quenched with 0.5M HCl (30 mL). The mixture was then extracted with dichloromethane one time and then brine was added. The precipitate was filtered and dried to give tert-butyl 2-(4-chlorobenzylamino)ethylcarbamate (3.58 g, 90%), MS (ESI) m/e (M+H+) 285.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846683B2
Source datasetuspto-grants-2014_09
ORD IDord-394bbebeab5740ebb021c6385dbd8b9e
Source noteuspto-grants-2014_09