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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776898Generated: November 2, 2026

Water → 3-(3-(Benzyloxy)-6-chloropyridin-2-yl)prop-2-yn-1-ol

https://huagongshe.com/reaction/1776898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropargyl alcoholHCID 7859—
Reactant3-(Benzyloxy)-6-chloro-2-iodopyridineHCID 58731010—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product3-(3-(Benzyloxy)-6-chloropyridin-2-yl)prop-2-yn-1-olHCID 8672828391.3%

Reaction Steps

A mixture of compound 3-(benzyloxy)-6-chloro-2-iodopyridine (2.5 g, 7.2 mmol), prop-2-yn-1-ol (443 mg, 7.9 mmol), Pd(PPh3)2Cl2 (280 mg, 0.4 mmol) and CuI (76 mg, 0.4 mmol) in Et3N (25 mL) was stirred at room temperature for 6 hours. Water (50 mL) was added and the mixture was extracted with dichloromethane. The organic layer was washed with brine and dried over Na2SO4. After concentrated, the resulting residue was purified using column chromatography (petroleum ether:ethyl acetate=2:1) to provide the product of compound 3-(3-(benzyloxy)-6-chloropyridin-2-yl)prop-2-yn-1-ol (1.8 g, yield: 90%). 1H-NMR (CDCl3, 400 MHz) δ 7.42˜7.33 (m, 5H), 7.17 (s, 2H), 5.18 (s, 2H), 4.54 (s, 2H). MS (M+H)+: 274/276.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265773B2
Source datasetuspto-grants-2016_02
ORD IDord-68abb589bdcb4926ac0829e6e047f236
Source noteuspto-grants-2016_02