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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706487Generated: October 30, 2026

Thionyl Chloride → HCID 118114064, compound

https://huagongshe.com/reaction/706487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 102546535HCID 102546535—
SolventDichloromethaneHCID 6344—
ProductHCID 118114064HCID 11811406481%

Reaction Steps

To a stirred solution of 1-(6-methoxypyridin-3-yl)propan-1-ol (1.67 g, 9.99 mmol) in dichloromethane (30 mL) at 0° C. was added thionyl chloride (2.46 g, 1.5 mL, 20.68 mmol). The cooling bath was removed, and the mixture was allowed to warm to room temperature. After 1 h, the reaction was quenched by the addition of saturated aqueous sodium bicarbonate solution. The phases were separated, and the organic phase was washed with brine (20 mL), dried over sodium sulfate, filtered, and concentrated to provide 1.50 g (81%) of 5-(1-chloropropyl)-2-methoxypyridine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174986B2
Source datasetuspto-grants-2015_11
ORD IDord-3d12ea5e5b3d45daa9200ee9c6120082
Source noteuspto-grants-2015_11