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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917401Generated: October 26, 2026

Triethylamine → 6,6-Difluoro-5-methyl-5-hexenyl methanesulfonate

https://huagongshe.com/reaction/917401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantMethyl 6,6-difluoro-5-methyl-5-hexenolHCID 23020199—
SolventTetrahydrofuranHCID 8028—
Product6,6-Difluoro-5-methyl-5-hexenyl methanesulfonateHCID 2302037199.6%

Reaction Steps

To 100 ml of tetrahydrofuran, 5.00 g (33 mmol) of methyl 6,6-difluoro-5-methyl-5-hexenol and 4.20 g (37 mmol) of methanesulfonyl chloride were dissolved, followed by drop-wisely adding 4.40 g (44 mmol) of triethylamine under ice-cooling. After the end of the drop-wise addition, the reaction liquid was stirred at room temperature for 1 hour. Hydrochloric acid salt of triethylamine was filtered, followed by adding water to the filtrate and extracting with ethyl acetate. The organic layer was washed with water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentrating under reduced pressure to obtain 7.50 g (yield: 99%) of 6,6-difluoro-5-methyl-5-hexenyl methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273878B2
Source datasetuspto-grants-2007_09
ORD IDord-002d529bf0d3487ebd5e33d89e7c7885
Source noteuspto-grants-2007_09