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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381851Generated: November 3, 2026

Methanesulfonyl chloride → HCID 13559066, compound

https://huagongshe.com/reaction/1381851

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. (IR: ν=1345, 1180 cm-1). ##STR45##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04804659
Source datasetuspto-grants-1989_02
ORD IDord-8406f592d403461eaac7a329a6340d7c
Source noteuspto-grants-1989_02