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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788640Generated: November 1, 2026

Methanesulfonyl chloride → HCID 20189890, compound

https://huagongshe.com/reaction/1788640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Propylbutane-1,4-diolHCID 12508255—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 20189890HCID 20189890—

Reaction Conditions

Temperature0 °C

Reaction Steps

Methanesulphonyl chloride (16.95 g) was added dropwise to a stirred solution of 3-hydroxymethylhexan-1-ol (8.94 g) in pyridine (39.5 g), maintaining the temperature at less than 5° C. Following the addition, the reaction mixture was stirred at 0° C. for 1.5 hours, then diluted with water and extracted with dichloromethane. The extracts were washed successively with water, dilute hydrochloric acid (X 2), water, aqueous sodium bicarbonate, and water, then dried over magnesium sulphate and concentrated to give 3-methanesulphonyloxymethylhex-1-yl methanesulphonate. (16.13 g, 83%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04684396
Source datasetuspto-grants-1987_08
ORD IDord-b735e5a5475e4b5385211bc2dd514f1b
Source noteuspto-grants-1987_08