Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | (4-Chlorophenyl)hydrazine | HCID 70624 | — |
| Reactant | 2-Chloro-4-dodecylsulfonylaniline | HCID 10861303 | — |
| Reactant | HCID 19938995 | HCID 19938995 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178443319 | HCID 178443319 | — |
Reaction Steps
A stirred mixture of 2-chloro- 4-dodecylsulfonylaniline (21.9 g, 0.061 moles), ethyl 3,3,3-trimethoxypropionate (11.7 g, 0.061 moles) and toluene (100 ml) was heated in an oil-bath at 110° C. until solution was attained. Concentrated sulfuric acid (4 drops) was added and the stirred mixture was heated for 2-25 hours allowing volatiles to distill off. The solution was cooled and the solvent was removed on the rotavapor to leave an oil. The oil was dissolved in glacial acetic acid (100 ml) and 4-chlorophenylhydrazine (8.7 g, 0.061 moles) was added. The mixture was stirred at room temperature for 22 hours. Then the resulting solid was filtered off, washed with methanol and dried. The solid was purified by trituration with ethyl acetate to give the product as a pale yellow solid weighing 20.1 g (60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05667946 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-0e43ab36f34b42e08e65d77367c0b4c4 |
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| Source note | uspto-grants-1997_09 |
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