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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866550Generated: November 2, 2026

Trifluoroacetic acid → 3-[3-(2-Amino-2-methyl-propyl)phenyl]-acrylic acid benzyl ester

https://huagongshe.com/reaction/1866550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-[3-(2-tert-Butoxycarbonylamino-2-methyl-propyl)-phenyl]-acrylic acid benzyl esterHCID 69023502—
SolventDichloromethaneHCID 6344—
Product3-[3-(2-Amino-2-methyl-propyl)phenyl]-acrylic acid benzyl esterHCID 69026130—

Reaction Steps

A mixture of 3-[3-(2-tert-butoxycarbonylamino-2-methyl-propyl)-phenyl]-acrylic acid benzyl ester (preparation 141), (2.23 g, 5.45 mmol), and trifluoroacetic acid (5 mL) in dichloromethane (10 mL) was stirred for 1 hour at room temperature. The mixture was then concentrated in vacuo and the residue was diluted with sodium hydrogen carbonate solution (10 mL) and extracted with ethyl acetate (3×20 mL). The combined organic solution was dried over magnesium sulfate and concentrated in vacuo to afford the title compound as a yellow oil in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629358B2
Source datasetuspto-grants-2009_12
ORD IDord-3506092baba04f239831d82bb5456718
Source noteuspto-grants-2009_12