Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496167Generated: October 27, 2026

Pyridine → 1-(Mesyloxymethyl)cyclohexanecarboxaldehyde

https://huagongshe.com/reaction/496167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-(Hydroxymethyl)-cyclohexanecarboxaldehydeHCID 13106397—
SolventDichloromethaneHCID 6344—
Product1-(Mesyloxymethyl)cyclohexanecarboxaldehydeHCID 2232526177.8%

Reaction Steps

To a cold (0° C. mixture of alcohol 54 (75 g, 0.54 mole) and 65.29 g (0.57 mole) of methanesulfonyl chloride in 80 ml of methylene chloride was added a solution of pyridine (47.96 g, 0.57 mole) in 40 ml of methylene chloride. The reaction mixture was stirred at room temperature for 18 h then quenched with water, acidified with conc. HCl and extracted with methylene chloride. The organic layer was washed with water, brine, and dried over sodium sulfate and concentrated under vacuum to give 91.63 g (77.8%) of thick oil. Proton NMR and mass spectra were consistent with the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943189B2
Source datasetuspto-grants-2005_09
ORD IDord-45dafcdbb98245a18e5c1716b6289a95
Source noteuspto-grants-2005_09