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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522718Generated: October 25, 2026

Methanesulfonyl chloride → (1-Methylcyclopropyl)methyl methanesulfonate

https://huagongshe.com/reaction/522718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(1-Methylcyclopropyl)methanolHCID 137701—
SolventDichloromethaneHCID 6344—
Product(1-Methylcyclopropyl)methyl methanesulfonateHCID 1363845296%

Reaction Conditions

Temperature0 °C

Reaction Steps

Treat a cooled solution (0° C.) of 1-methylcyclopropanemethanol (2.0 g, 23.22 mmol) in DCM (75 mL) with TEA (2.58 g, 25.5 mmol) and add methanesulfonyl chloride (2.93 g, 25.5 mmol) dropwise. Stir the mixture at 0° C. for 2 h, wash with H2O then brine, dry over Na2SO4 and concentrate to dryness to afford the title compound (3.66 g, 96%) as an oil. 1H NMR (400 MHz, DMSO-d6): δ 3.60 (s, 3H), 2.10 (m, 2H), 0.72 (s, 3H), 0.14 (m, 2H), 0.01 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334267B2
Source datasetuspto-grants-2016_05
ORD IDord-8f9522bda5f74728bf876b0552e60e0f
Source noteuspto-grants-2016_05