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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477096Generated: October 30, 2026

Methanesulfonyl chloride → HCID 90285103, compound

https://huagongshe.com/reaction/1477096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant(R)-(-)-6-Methyl-5-hepten-2-olHCID 6971128—
SolventDichloromethaneHCID 6344—
ProductHCID 90285103HCID 9028510388.8%

Reaction Conditions

Temperature5 °C

Reaction Steps

(R)-6-Methyl-hept-5-en-2-ol (1) (2.26 g, 17.6 mmol) and DIEA (5.52 mL, 31.7 mmol) were dissolved in anhydrous DCM (24 mL), the reaction mixture was cooled to 5° C., mesyl chloride (1.64 mL, 21.1 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 (60 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 (3.225 g, 86%). H1 NMR: see supporting information. TLC, Hexane-DCM-EtOAc, 40:40:20, 2 Rf 0.70 (developed with KMnO4 stain). 1H NNMR in CDCl3 (500 MHz): 5.08 ppm 1 Hm, 4.80 ppm 1 Hm, 2.99 ppm 3 Hs, 2.08 ppm 2 Hm, 1.75 ppm 1 Hm, 1.69 ppm 3 Hs, 1.624 1 Hm, 1.61 3 Hs, 1.43 ppm 3 Hd.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403755B2
Source datasetuspto-grants-2016_08
ORD IDord-b4919164fde14c338bbebb070c9055e5
Source noteuspto-grants-2016_08