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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100397Generated: November 2, 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/2100397

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
Reactant(5-Chloro-2-iodophenyl)(2,6-difluorophenyl)methanoneHCID 46835488—
CatalystHCID 178418476HCID 178418476—
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 numberUS07572784B2
Source datasetuspto-grants-2009_08
ORD IDord-1bec7743c27d402180a2b13da1867253
Source noteuspto-grants-2009_08