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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866549Generated: October 29, 2026

Triethylamine → 3-[3-(2-tert-Butoxycarbonylamino-2-methyl-propyl)-phenyl]-acrylic acid benzyl ester

https://huagongshe.com/reaction/1866549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorous acid, tris(methylphenyl) esterHCID 12106—
ReactantBenzyl acrylateHCID 75617—
Reactanttert-butyl N-[1-(3-bromophenyl)-2-methylpropan-2-yl]carbamateHCID 58907464—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
Product3-[3-(2-tert-Butoxycarbonylamino-2-methyl-propyl)-phenyl]-acrylic acid benzyl esterHCID 6902350290%

Reaction Steps

A mixture of [2-(3-bromophenyl)-1,1-dimethylethyl]carbamic acid tert-butyl ester (preparation 32), (2 g, 6.09 mmol), benzyl acrylate (2 g, 12.19), palladium (II) acetate (204 mg, 0.91 mmol), tri-p-tolyl phosphite (556 mg, 1.83 mmol) and triethylamine (2.12 mL, 15.22 mmol) in acetonitrile (100 mL) was heated under reflux for 48 hours. The reaction mixture was then concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with ethyl acetate:pentane to afford the title compound as a pale yellow oil in 90% yield, 2.23 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629358B2
Source datasetuspto-grants-2009_12
ORD IDord-4a8fc45bb1ab419692edecb4baa98f76
Source noteuspto-grants-2009_12