HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091163Generated: November 1, 2026
Thionyl Chloride → 5-Chloro-2-(1-chloro-3-methylbutyl)-3-methyl-1-benzofuran
https://huagongshe.com/reaction/2091163
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66777421 | HCID 66777421 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Chloro-2-(1-chloro-3-methylbutyl)-3-methyl-1-benzofuran | HCID 66778446 | 96% |
Reaction Steps
To a solution (10 mL) of 1-(5-chloro-3-methyl-1-benzofuran-2-yl)-3-methylbutan-1-ol (650 mg) synthesized above in toluene was added thionyl chloride (225 μL), and the mixture was stirred at 50° C. for 2 hr. The reaction mixture was poured into ice-cooled saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give the title object compound (668 mg, 96%) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08436043B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-94c05cc2d0e544d29384b8c5df6a4ddb |
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| Source note | uspto-grants-2013_05 |
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