HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917364Generated: October 30, 2026
Tetrahydrofuran → HCID 86760553, compound
https://huagongshe.com/reaction/917364
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzo[b]thiophene-2-carbonyl Chloride | HCID 142384 | — |
| Reactant | HCID 23020242 | HCID 23020242 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86760553 | HCID 86760553 | 80% |
Reaction Steps
To 10 ml of tetrahydrofuran were dissolved 0.25 g (1.5 mmol) of 6,6-difluoro-5-methyl-5-hexene-1-thiol and 0.39 g (2.0 mmol) of benzo[b]thiophene-2-carbonylchloride, followed by the drop-wise addition of 0.30 g (3.0 mmol) of triethylamine at room temperature, followed by stirring at the same temperature for 1 hour. 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=1:20) to obtain 0.39 g (yield: 80%) of S-(6,6-difluoro-5-methyl-5-hexenyl) benzo[b]thiophene-2-thiocarboxylate.
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-1b1ea18222b7412aa1de274de4b314ed |
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| Source note | uspto-grants-2007_09 |
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