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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433155Generated: October 31, 2026

Triethylamine → N-[3-benzyloxy-4-(2-bromo-acetyl)phenyl]-acetamide

https://huagongshe.com/reaction/1433155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantDiethylphosphiteHCID 3780918—
ReactantN-[3-benzyloxy-4-(2,2-dibromo-acetyl)phenyl]-acetamideHCID 85978776—
SolventTetrahydrofuranHCID 8028—
ProductN-[3-benzyloxy-4-(2-bromo-acetyl)phenyl]-acetamideHCID 85606679118.9%

Reaction Steps

A solution of diethylphosphite (12.6 μL, 13.5 mg, 97.6 μmol) and triethylamine (13.6 μL, 9.9 mg, 97.6 μmol) in THF (0.1 mL) was added to a stirred solution of N-[3-benzyloxy-4-(2,2-dibromo-acetyl)-phenyl]-acetamide (41 mg, 92.9 μmol) in THF (1.5 mL) at room temperature, and the reaction stirred for 2 hours. The mixture was poured into EtOAc (20 mL) and washed with water (20 mL) and brine (20 mL). The organic layer was dried (MgSO4) and the solvent removed in vacuo to give N-[3-benzyloxy-4-(2-bromo-acetyl)-phenyl]-acetamide (40 mg, >100%), which was seen by NMR to be contaminated with a diethylphosphite-derived contaminant. The material could be used successfully in the following steps without further purification. All analytical data was as reported above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612201B2
Source datasetuspto-grants-2009_11
ORD IDord-e93ff9415bc248818b994272a26f7c21
Source noteuspto-grants-2009_11