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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477100Generated: November 4, 2026

Methanesulfonyl chloride → HCID 90286347, compound

https://huagongshe.com/reaction/1477100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-(+)-6-Methyl-5-hepten-2-olHCID 6971127—
SolventDichloromethaneHCID 6344—
ProductHCID 90286347HCID 9028634776%

Reaction Conditions

Temperature5 °C

Reaction Steps

(S)-6-Methyl-hept-5-en-2-ol (2.64 g, 20.58 mmol) and DIEA (6.45 mL, 37.0 mmol) were dissolved in anhydrous DCM (28 mL), the reaction mixture was cooled to 5° C., mesyl chloride (1.91 mL, 24.7 mmol) was added dropwise, and the reaction mixture was allowed to slowly warm to RT. After 18 h at RT the reaction mixture was diluted with DCM (100 mL), washed with water (3×35 mL), brine (35 mL), dried with MgSO4, solvent was concentrated to give a dark oil which was purified by SiO2 flash chromatography using Hexane-EtOAc to give the title compound as an oil (3.213 g, 76%). TLC, Hexane-DCM-EtOAc, 40:40:20, 2 Rf 0.70 (developed with KMnO4 stain). H1 NMR (CDCl3): • 5.08 (m, 1H), 4.80 (m, 1H), 2.99 (s, 3H), 2.10 (m, 2H), 1.75 (m, 1H), 1.69 (s, 3H), 1.62 (m, 1H), 1.61 (s, 3H), 1.43 (d, 3H, J=6.5 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403755B2
Source datasetuspto-grants-2016_08
ORD IDord-6105d5a6651145509d27cc6cc308d8c9
Source noteuspto-grants-2016_08