Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminobiphenyl | HCID 7102 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 2747686 | HCID 2747686 | 73% |
Reaction Steps
To a stirring solution of 4-aminobiphenyl (9.53 g, 56.3 mmol) and triethylamine (5.70 g, 56.3 mmol, 7.85 mL) in methylene chloride (60 mL), cooled to 0° C., was added slowly isobutyryl chloride (6.0 g, 56.3 mmol, 5.90 mL). After stirring at 0° C. for 1 h, the mixture was diluted with methylene chloride (120 mL) and washed with 1 N NaOH and saturated brine, then dried (MgSO4), filtered and concnetrated. The residue was washed with ether and dried to provide the title compound as a pale yellow crystalline solid (9.83 g, 73%). 1HNMR (400 MHz, CDCl3/CD3OD) δ7.58 (d, 2H), 7.50 (m, 4H), 7.40-7.25 (m, 3H), 2.55-2.49 (m, 1H), 1.18 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06232342B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-31b358fa55db4d3995347e5fdf482158 |
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| Source note | uspto-grants-2001_05 |
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