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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzo(b)thiophene-2-carboxylic acid | HCID 95864 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6,6-Difluoro-5-methyl-5-hexenyl methanesulfonate | HCID 23020371 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6,6-Difluoro-5-methyl-5-hexenyl benzo[b]thiophene-2-carboxylate | HCID 69181690 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07273878B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-9db6e71ddd914462931406307e242912 |
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| Source note | uspto-grants-2007_09 |
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