Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 131723967 | HCID 131723967 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 91032561 | HCID 91032561 | 98.5% |
Reaction Steps
1-Phenyl-5-propyl-1H-pyrazole-4-carboxylic acid (6-hydroxy-naphthalen-2ylmethyl)-methyl-amide (3.2 g, 8 mmol), prepared in the previous step, was dissolved in 300 mL glacial acetic acid (with warming). A solution of bromine (0.41 mL, 8 mmol) in 50 mL of glacial acetic acid was added under nitrogen dropwise over 2 h to the reaction at room temperature. After the addition the reaction stirred for 2 days. The solvent was removed under reduced pressure and the residue diluted with methylene chloride. The organic layer was extracted two times with 5% NaHCO3, dried (MgSO4) and the solvent removed under reduced pressure to give 1-phenyl-5-propyl-1H-pyrazole-4-carboxylic acid (5-bromo-6-hydroxy-naphthalen-2-ylmethyl)-methyl-amide (3.77 g, 98.5%) as a pink solid, mp 205-207° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06589970B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-a297327696704be694cc8fca5ae3bed9 |
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| Source note | uspto-grants-2003_07 |
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