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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285376Generated: October 31, 2026

Pyridine → Methanesulfonate

https://huagongshe.com/reaction/1285376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzenemethanol, .alpha.-ethyl-4-methoxy-HCID 92218—
SolventDichloromethaneHCID 6344—
Product3-(4-Methoxyphenyl)-1-propanolHCID 79406—
ProductMethanesulfonateHCID 85257421.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methyl sulphonyl chloride (12.5 g, 0.11M) was added dropwise to a stirred solution of p-methoxyphenylpropanol (16.6 g, 0.10M) in dichloromethane (60 ml)/pyridine (20 ml) at 0° C. The reaction mixture was maintained at 0° C. for 12 hours, then diluted with dichloromethane (250 ml) and washed with hydrochlorid acid (5×50 ml of 5 M.l-1). The solution was washed with water, dried (MgSO4) and the solvent was evaporated off under reduced pressure to give 3-(4-methoxyphenyl)propan-1-ol, methane sulphonate (20 g), as a colourless crystalline solid, m.p. 41°-42° C. (pentane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04567189
Source datasetuspto-grants-1986_01
ORD IDord-f963ce5269e34a779ad236555fd10cf3
Source noteuspto-grants-1986_01