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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785428Generated: October 26, 2026

{2-[3-(Benzhydrylidene-amino)-phenyl]-1-methyl-ethyl}-carbamic acid tert-butyl ester → 3-(2-Aminopropyl)aniline

https://huagongshe.com/reaction/1785428

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{2-[3-(Benzhydrylidene-amino)-phenyl]-1-methyl-ethyl}-carbamic acid tert-butyl esterHCID 86600374—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product3-(2-Aminopropyl)anilineHCID 20442370—

Reaction Steps

A solution {2-[3(Benzhydrylidene-amino)-phenyl]-1-methyl-ethyl}-carbamic acid tert-butyl ester (200 mg, 0.48 mmol) in dichloromethane (5 mL) and trifluoroacetic acid (5 mL) was stirred for 45 min at room temperature. Solvents removed under vacuum and residue suspended in 5 N hydrochloric acid at 60° C. for 20 min. Biphasic system washed with ether and organics discarded. The pH of the aqueous layer was then adjusted to 14 with 10 N sodium hydroxide. Aqueous was then washed three times with dichloromethane (10 mL). Combined organics dried over magnesium sulfate, and product isolated as an amber film after removal of solvent under vacuum. M+1=151.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504403B2
Source datasetuspto-grants-2009_03
ORD IDord-8ecacdfd807041be80650c8a448f0c32
Source noteuspto-grants-2009_03