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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097571Generated: October 27, 2026

Methanol → 2-(Azetidin-3-yloxy)-5-iodo-pyridine hydrochloride

https://huagongshe.com/reaction/2097571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactant2-(1-Benzhydryl-azetidin-3-yloxy)-5-iodo-pyridineHCID 58073101—
SolventDichloromethaneHCID 6344—
Product2-(Azetidin-3-yloxy)-5-iodo-pyridine hydrochlorideHCID 66710162109.5%

Reaction Steps

1-chloroethyl chloroformate (12.8 mL, 0.104 mol) was added drop-wise via syringe to a stirred solution of 2-(1-Benzhydryl-azetidin-3-yloxy)-5-iodo-pyridine (23.03 g, 0.052 mol) in dichloromethane (250 mL) at ambient temperature. The resulting solution was stirred at ambient temperature for 3.5 hr, then methanol (250 mL) was added and the reaction mixture stirred at ambient temperature for 16 hr. The solvents were then removed in vacuo and the resulting solid residue was triturated with diethyl ether, filtered and then dried in vacuo to afford the title product as a cream-coloured solid (17.8 g, >quant yield). The crude product was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450346B2
Source datasetuspto-grants-2013_05
ORD IDord-01f449fd5b4142acaf961016225f383c
Source noteuspto-grants-2013_05