Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chloral Hydrate | HCID 2707 | — |
| Reactant | 3-Fluoro-4-methylaniline | HCID 9957 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Hydroxylamine, sulfate (1:1) | HCID 159255 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 72486482 | HCID 72486482 | 94.4% |
Reaction Steps
To a solution of chloral hydrate (2.97 g, 17.98 mmol) and anhydrous sodium sulfate (15.20 g, 107 mmol) in water (50 mL) add a mixture of hydroxylamine sulfate (13.67 g, 83.23 mmol), 3-Fluoro-4-methyl-phenylamine (2 g, 15.98 mmol), concentrated hydrochloric acid (1.67 mL) in water (17 mL). Heat the mixture at 45° C. for 2 h and at 75° C. for 1 hr. Cool the mixture to room temperature and filter the solid. Wash the solid with water and ethyl ether. Dry the solid under vacuum to yield the title compound (2.96 g, 94%). 1H NMR (DMSO-d6, 300 MHz) δ 2.08 (d, J=1.0 Hz, 3H), 7.12 (t, J=8.8 Hz, 1H), 7.25 (dd, J=2.1, 8.2 Hz, 1H), 7.36 (dd, J=1.6, 12.4 Hz, 1H), 10.18 (s, 1H), 12.11 (s, 1H). MS (ES−): 195 (M−H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07749992B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-511721a1eeab493b99a052e43804a793 |
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| Source note | uspto-grants-2010_07 |
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