HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192886Generated: October 31, 2026
Water → 1-Bromo-2-(cyclopropylsulfanyl)benzene
https://huagongshe.com/reaction/2192886
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromocyclopropane | HCID 78037 | — |
| Reactant | 2-Bromobenzenethiol | HCID 80598 | — |
| Catalyst | Benzenemethanethiol, alpha,alpha-diphenyl- | HCID 77281 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Bromo-2-(cyclopropylsulfanyl)benzene | HCID 59570916 | 81.4% |
Reaction Steps
To a solution of 2-bromobenzenethiol (50 g) in DMF (500 mL) were added bromocyclopropane (41.6 g), potassium carbonate (54.8 g), and triphenylmethanethiol (1.46 g), followed by stirring at an internal temperature of 80° C. for 24 hours. After cooling to room temperature, water and ethyl acetate were added thereto, and the organic layer was then separated. The organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 1-bromo-2-(cyclopropylsulfanyl)benzene (49.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329707B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-68b7b06613c94dab94e85492a5bc94aa |
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| Source note | uspto-grants-2012_12 |
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