Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Isopropylaniline | HCID 7464 | — |
| Reactant | 3-Methyl-2-butenoyl chloride | HCID 102394 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19177440 | HCID 19177440 | — |
Reaction Steps
To a solution of 4-isopropylaniline (5.0 g, 37.0 mmol) in 100 ml of anhydrous CH2Cl2 under argon at 0° C. was added 3,3-dimethylacryloyl chloride (4.12 ml, 37.0 mmol). Pyridine (3.0 ml, 40.6 mmol) was added, and the mixture was stirred at 25° C. for 12 hours. The reaction was quenched with water and extracted with ethyl ether. The organic layer was washed with water, and brine, dried over Na2SO4 and were in vacuo to give the title compound as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06734193B1 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-7d8b6fa59a8e4bcab820737676d953a9 |
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| Source note | uspto-grants-2004_05 |
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