Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 70393299 | HCID 70393299 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70393690 | HCID 70393690 | 46.4% |
Reaction Steps
To a stirred solution of monomethylamine (50 ml, 1.13 mol) in 150 ml of methanol at 0° C. under nitrogen, was added 2-chloro-N-[(1,2-diphenyl-1-(trifluoromethyl)ethyl]acetamide (from Example 1) (10.2 g) followed by 100 ml of methanol to effect solution. The mixture was allowed to slowly warm to ambient temperature and stirred for 24 hours. The solvent was evaporated and the resulting semi-solid was dissolved in 150 ml of chloroform, 100 ml of water and 20 ml of 15% NaOH. The phases were separated, the aqueous phase extracted with chloroform (2×125 ml) and the combined organic phases washed with brine (150 ml), decolorized with charcoal, dried and evaporated to a yellow-orange oil, 9.8 g. This was dissolved in 150 ml of methanol, treated with 3.4 g of maleic acid and the solvent removed under vacuum to yield a solid which was recrystallized from methanol (150 ml) and ethyl acetate (150 ml), then from methanol (30 ml) and ethyl acetate (75 ml) and vacuum dried to give 4.88 g of 2-(methylamino)-N-[1,2-diphenyl-1-(trifluoromethyl)ethyl]acetamide maleate as a white solid, mp 179°-181° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04798687 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-aede2fbdb7894cf2b144e7e30f009c3c |
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| Source note | uspto-grants-1989_01 |
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