Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | 3-Bromophenylhydrazine hydrochloride | HCID 33757 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86620836 | HCID 86620836 | 97.1% |
Reaction Steps
(3-Bromophenyl)hydrazine hydrochloride (10 g, 44 mmol, 1 eq.), benzophenone (8.14 g, 44 mmol, 1 eq.) and ethanol (100 mL) are placed in a 250 mL round-bottomed flask. 2 mL of concentrated sulfuric acid are then added. The resulting suspension is heated at a temperature in the region of 80° C. After 30 minutes at this temperature, the suspension becomes a solution. The solution is stirred at this temperature for 18 hours, and is then concentrated to 95%. The residue is diluted with ethyl acetate and washed with sodium hydrogen carbonate solution. After drying over magnesium sulfate, the solution is concentrated and the residue is purified by chromatography on a column of silica gel, eluting with an ether/heptane mixture (3/97 by volume). 15 g (95%) of N-benzhydrylidene-N′-(3-bromophenyl)hydrazine are thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07595320B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-4837983e3ee9403d9fcb8d2f61122bb4 |
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| Source note | uspto-grants-2009_09 |
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