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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606892Generated: November 1, 2026

Methanesulfonyl chloride → HCID 13559066, compound

https://huagongshe.com/reaction/1606892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 13559064HCID 13559064—
SolventPyridineHCID 1049—
ProductHCID 13559066HCID 1355906666%

Reaction Steps

11 g (0.1 mol) of methanesulphonyl chloride are added dropwise, with stirring at 0° C. to 14 g (0.074 mol) of 2-methyl-3-β-naphthylpropanol (crude) in 80 ml of absolute pyridine, the mixture is stirred for a further 16 hours at room temperature after the addition is complete, excess pyridine is removed by distillation in vacuo, the residue is taken up in water, extracted repeatedly with dichloromethane and dried over sodium sulphate, and the solvent is removed in vacuo. 13.6 g (66% of theory) of 1-methanesulphonyloxy-2-methyl-3-β-naphthyl-propane are obtained as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863917
Source datasetuspto-grants-1989_09
ORD IDord-dd62a20dc7f441fc8e9b1b674a609fe2
Source noteuspto-grants-1989_09