Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | alpha-(4-chlorophenyl)-1-methyl-1H-benzotriazole-6-methanol | HCID 14990605 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178419576 | HCID 178419576 | 76.6% |
Reaction Steps
A mixture of 245 parts of α-(4-chlorophenyl)-1-methyl-1H-benzotriazole-6-methanol and 1500 parts of a hydrobromic acid solution in acetic acid was stirred for 2.5 hours at 40° C. The reaction mixture was evaporated at 60° C. and the residue was stirred in dichloromethane. After cooling to 10° C., the precipitated product was filtered off and dried, yielding 285 parts (76.6%) of 6-[bromo(4-chlorophenyl)methyl]-1H-benzotriazole monohydrobromide (int. 130).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04943574 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-e3db621848584cae8702e3534f34c8cd |
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| Source note | uspto-grants-1990_07 |
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