Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Reactant | HCID 135592938 | HCID 135592938 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 135592939 | HCID 135592939 | — |
Reaction Steps
A stirred mixture of 5-(2-hydroxyphenyl)benzofurazan (11.2 g, 52.8 mmol), and tetrabutylammonium tribromide (25.5 g, 52.8 mmol) in dichoromethane (530 mL) is stirred at 18° C. for 18 h. The solvent is evaporated off under reduced pressure to yield a residue which is treated with water (300 mL) and extracted with ethyl acetate (3×100 mL). The combined extracts are washed (saturated NaCl), dried (Na2SO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by recrystallisation from ethyl acetate-hexane to give 5-(3-bromo-6-hydroxyphenyl)benzofurazan as a pale-yellow crystalline solid, m.p. 179-181° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258843B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-7edd3f672c5f4063922229edac43ed72 |
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| Source note | uspto-grants-2001_07 |
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