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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513125Generated: November 1, 2026

tert-butyl N-(prop-2-yn-1-yl)carbamate → tert-Butyl (3-(4-chloro-2-(2,6-difluorobenzoyl)phenyl)prop-2-yn-1-yl)carbamate

https://huagongshe.com/reaction/513125

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
Reactant(5-Chloro-2-iodophenyl)(2,6-difluorophenyl)methanoneHCID 46835488—
SolventDichloromethaneHCID 6344—
Producttert-Butyl (3-(4-chloro-2-(2,6-difluorobenzoyl)phenyl)prop-2-yn-1-yl)carbamateHCID 52911151—

Reaction Steps

(5-Chloro-2-iodo-phenyl)-(2,6-difluoro-phenyl)-methanone (2aa) (5.5 g, 14.5 mmol), prop-2-ynyl-carbamic acid tert-butyl ester (2.5 g, 16 mmol), PdCl2 (PPh3)2 (0.6 g, 0.9 mmol) and Cu(I)I (0.2 g, 0.9 mmol) were suspended in anhydrous CH2Cl2 (50 mL) and the mixture was sparged with nitrogen for 30 min. Diethylamine (8 mL) was added and the solution was stirred at room temperature for 16 h. The solution was concentrated in vacuo and the resulting residue purified by column chromatography (silica gel, 0 to 15% EtOAc/hexanes) to afford 3aa (3.6 g, 61%) as a white solid, MS m/z=406 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102678B2
Source datasetuspto-grants-2015_08
ORD IDord-79b7c6c170304aa690d53614a72d3fbb
Source noteuspto-grants-2015_08