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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441139Generated: October 29, 2026

Water → 1-methanesulfonyl-4-(S)-methyl-8-methylnon-7-ene

https://huagongshe.com/reaction/441139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-(S)-methyl-8-methylnon-7-enyl alcoholHCID 11171229—
SolventDichloromethaneHCID 6344—
Product1-methanesulfonyl-4-(S)-methyl-8-methylnon-7-eneHCID 22861490—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-(S)-methyl-8-methylnon-7-enyl alcohol (3.25 g, 19.1 mmol) in dichloromethane (50 ml) at 0° C. was added methanesulfonyl chloride (2.29 g, 20.0 mmol) followed by triethylamine (3.04 g, 30.0 mmol) After stirring for 10 min at 0° C., the reaction was allowed to warm to 25° C. and stirred for 3 hr. The reaction was poured into water (50 ml), separated and washed with dichloromethane (50 ml). The organic portions were combined, dried (magnesium sulfate), and evaporated to give the 1-methanesulfonyl-4-(S)-methyl-8-methylnon-7-ene as a yellow oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521315
Source datasetuspto-grants-1996_05
ORD IDord-78dbb138de94491aa51915d8e9a7ccff
Source noteuspto-grants-1996_05