Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanethiol | HCID 8012 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,2-Dibromo-1,1,2,2-tetrafluoroethane | HCID 31301 | — |
| Reactant | 2-BROMO-6-FLUOROPHENOL | HCID 2779284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 90414055 | HCID 90414055 | 76.5% |
Reaction Steps
2-Bromo-6-fluorophenol (10.2 g, 53 mmol), potassium carbonate (7.3 g, 53 mmol), 1,2-dibromo-tetrafluoroethane (21 g, 80 mmol) and 1-butanethiol (1.1 g, 12 mmol) were combined in dry N,N-dimethylformamide (75 mL) and heated to 50° C. in a stirred pressure reactor. After cooling, the contents were mixed with 1.0 M sodium hydroxide (NaOH; 100 mL) and extracted three times with diethyl ether (80 mL portions). The combined extracts were washed with water (15 mL), 2.0 M NaOH (45 mL), dried (Na2SO4) and concentrated by rotary evaporation. The material was purified by silica gel chromatography eluting with hexane to afford the title compound as a clear liquid (15 g, 76%): 1H NMR (400 MHz, CDCl3) δ 7.48-7.39 (m, 1H), 7.22-7.14 (m, 2H); EIMS m/z 368.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09149038B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-abcfd28db41d491a8c69383a55980740 |
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| Source note | uspto-grants-2015_10 |
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