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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221409Generated: October 30, 2026

{3-[1-[tert-Butoxycarbonyl-(2-methoxy-ethyl)-amino]-2-(tert-butyl-dimethyl-silanyloxy)ethyl]-phenyl}-carbamic acid benzyl ester → tert-Butyl 1-(3-aminophenyl)-2-(tert-butyldimethylsilyloxy)ethyl(2-methoxyethyl)carbamate

https://huagongshe.com/reaction/221409

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{3-[1-[tert-Butoxycarbonyl-(2-methoxy-ethyl)-amino]-2-(tert-butyl-dimethyl-silanyloxy)ethyl]-phenyl}-carbamic acid benzyl esterHCID 67329507—
SolventHydrochloric AcidHCID 313—
Producttert-Butyl 1-(3-aminophenyl)-2-(tert-butyldimethylsilyloxy)ethyl(2-methoxyethyl)carbamateHCID 58378837—

Reaction Steps

{3-[1-[tert-Butoxycarbonyl-(2-methoxy-ethyl)-amino]-2-(tert-butyl-dimethyl-silanyloxy)ethyl]-phenyl}-carbamic acid benzyl ester was added to ethanolic HCl (20 mL) at 0° C., allowed to warm to room temperature and stirred overnight. The reaction mixture was concentrated to give the title compound as a light yellow oil (300 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207167B2
Source datasetuspto-grants-2012_06
ORD IDord-d101d3fdc9f9422e883fa73150dc9dd6
Source noteuspto-grants-2012_06