Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 1,1,2,2-Tetrachloroethane | HCID 6591 | — |
| Reactant | HCID 66611520 | HCID 66611520 | — |
| Catalyst | Manganese oxide | HCID 160959 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66614304 | HCID 66614304 | — |
Reaction Steps
To a mixture of 4-(2,6-difluorophenyl)-3-buten-2-one (i.e. the product of Step A) (8.1 g, 44.5 mmol) in ethanol (50 mL) was added methylhydrazine (2.1 g, 49 mmol). After 24 h, the reaction mixture was concentrated under reduced pressure. To the resulting oil (10.1 g) was added 1,1,2,2-tetrachloroethane (65 mL) and manganese oxide (41.7 g, 480 mmol). The reaction mixture was heated at 140° C. for 20 minutes, and then cooled to room temperature and filtered through a pad of Celite® (diatomaceous earth) on a sintered glass frit funnel rinsing with dichloromethane (2×20 mL). The filtrate was concentrated under reduced pressure and the resulting material was purified by MPLC (10 to 50% gradient of ethyl acetate in hexanes as eluant) to provide the title compound as a light yellow solid (4.02 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09131693B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-5a40f3c0e0bf448896aa548e42012a32 |
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| Source note | uspto-grants-2015_09 |
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