HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638953Generated: November 2, 2026
Bromine → 4-Bromo-2-[(trifluoromethyl)sulfanyl]phenol
https://huagongshe.com/reaction/638953
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 33185-56-7 | HCID 10176507 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-2-[(trifluoromethyl)sulfanyl]phenol | HCID 68685673 | 93% |
Reaction Steps
To a stirred solution of 1-hydroxy-2-trifluoromethylthiobenzene (16 mmol, 1.0 eq.) in CH2Cl2 (40 mL) at −78° C. was added a solution of Br2 (0.83 mL, 16 mmol, 1.0 eq.) in CH2Cl2 (18 mL) slowly. The resulting mixture was stirred at −78° C. for 2 h and then warmed to room temperature overnight. The reaction mixture was diluted with water (300 mL) and extracted with CH2Cl2 (3×150 mL). The combined organic layer was washed with brine (400 mL), dried (Na2SO4) and concentrated in vacuo. The crude product was purified by column chromatography using 0-10% EtOAc in hexanes as an eluent to afford 4-bromo-1-hydroxy-2-trifluoromethylthiobenzene in 93% yield as a crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691843B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-ffeb37b852f64469997f16b077af38bf |
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| Source note | uspto-grants-2010_04 |
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