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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917352Generated: October 26, 2026

Dimethylformamide → 6,6-Difluoro-5-methyl-5-hexenyl benzo[b]thiophene-2-carboxylate

https://huagongshe.com/reaction/917352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzo(b)thiophene-2-carboxylic acidHCID 95864—
ReactantSodium BicarbonateHCID 516892—
Reactant6,6-Difluoro-5-methyl-5-hexenyl methanesulfonateHCID 23020371—
SolventWaterHCID 962—
Product6,6-Difluoro-5-methyl-5-hexenyl benzo[b]thiophene-2-carboxylateHCID 6918169081%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 40 ml of N,N-dimethylformamide were dissolved 5.00 g (22 mmol) of 6,6-difluoro-5-methyl-5-hexenyl methanesulfonate and 4.30 g (24 mmol) of benzo[b]thiophene-2-carboxylicacid, followed by the addition of 6.00 g (71 mmol) of sodium hydrogencarbonate and stirring at 100° C. for 3 hours. The reaction liquid was then poured in water and extracted with diethyl ether. The organic layer was washed with water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentration under reduced pressure. The residue was purified with silica gel column chromatography (diisopropyl ether:hexane=1:7) to obtain 5.50 g (yield: 81%) of 6,6-difluoro-5-methyl-5-hexenyl benzo[b]thiophene-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273878B2
Source datasetuspto-grants-2007_09
ORD IDord-9db6e71ddd914462931406307e242912
Source noteuspto-grants-2007_09