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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044015Generated: October 30, 2026

Ethynylcyclobutane → HCID 57908178, compound

https://huagongshe.com/reaction/1044015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthynylcyclobutaneHCID 142749—
Reactanttert-Butyl (6-chloro-4-iodopyridin-3-yl)carbamateHCID 53415320—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 57908178HCID 5790817860%

Reaction Conditions

Temperature25 °C

Reaction Steps

To the solution of tert-butyl 6-chloro-4-iodopyridin-3-ylcarbamate (7.0 g, 19.8 mmol) in Et3N (100 mL) was added the solution of ethynylcyclobutane in THF (prepared in step a), Pd(PPh3)2Cl2 (1.8 g, 2.1 mmol) and CuI (400 mg, 2.1 mmol). The reaction mixture was stirred at 25° C. for 16 h. The mixture was diluted with water and extracted with dichloromethane (3×100 mL). The extract was washed with brine, dried, concentrated in vacuo and purified by chromatography on silica gel (5-10% ethyl acetate in petroleum ether as eluant) to afford tert-butyl 6-chloro-4-(cyclobutylethynyl)pyridin-3-ylcarbamate (3.6 g, 60% yield). 1H NMR (300 MHz, CDCl3) δ: 9.11 (br, s, 1H), 7.22 (s 1H), 6.97 (s, 1H), 3.39-3.25 (m, 1H), 2.48-1.98 (m, 6H), 1.52 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563573B2
Source datasetuspto-grants-2013_10
ORD IDord-d78b6778637f40f4962bf3956da92f55
Source noteuspto-grants-2013_10