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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388290Generated: October 30, 2026

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

https://huagongshe.com/reaction/388290

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 numberUS08377937B2
Source datasetuspto-grants-2013_02
ORD IDord-125daede6bde40b5a5412b145d937e4e
Source noteuspto-grants-2013_02