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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761850Generated: October 29, 2026

Methanesulfonyl chloride → HCID 13559066, compound

https://huagongshe.com/reaction/1761850

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 to 14 g (0.074 mol) of 2-methyl-3-β-naphthylpropanol (crude) in 80 ml of absolute pyridine at 0° C., with stirring, the mixture is stirred at room temperature for a further 16 hours. When the addition has ended, excess pyridine is removed by distillation in vacuo, the residue is taken up in water, the mixture is extracted several times with methylene chloride, the extract is 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 numberUS04829063
Source datasetuspto-grants-1989_05
ORD IDord-57b400d83fa24a00b56d4972a90872f4
Source noteuspto-grants-1989_05