Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 4-Methyl-3-nitroaniline | HCID 8390 | — |
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 4941244 | HCID 4941244 | 50% |
Reaction Steps
To a solution of ammonium thiocyanate (1.05 g, 13.85 mmol) in acetone (21 mL) was added dropwise acetyl chloride (0.90 mL 12.70 mmol). The reaction mixture was stirred at 40° C. for 30 min. Then, a solution of 4-methyl-3-nitroaniline (1.76 g, 11.54 mmol) in acetone (7 mL) was added and the reaction mixture was stirred at room temperature for 4 h. The reaction mixture was poured into ice-water and the precipitate was filtered, washed with more water and cyclohexane to give compound IV-c as brown solid in 50% yield. (300 MHz, DMSO) δ 12.45 (s, 1H), 11.53 (s, 1H), 8.38 (d, J=2.0 Hz, 1H), 7.69 (dd, J=8.3, 2.0 Hz, 1H), 7.43 (d, J=8.3 Hz, 1H), 2.44 (s, 3H), 2.09 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09168245B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-c67a8e534f244d0b95dfc4fb4a6cd2e3 |
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| Source note | uspto-grants-2015_10 |
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