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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948856Generated: October 30, 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/1948856

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)7 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 numberUS08399659B2
Source datasetuspto-grants-2013_03
ORD IDord-49280cb0e5d44552be416770e14f8037
Source noteuspto-grants-2013_03