Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzhydrylamine | HCID 7036 | — |
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | HCID 18678940 | HCID 18678940 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 18678921 | HCID 18678921 | 23% |
Reaction Steps
Ethyl acrylate (1.05 g; 10.0 mmol) and diphenylmethyamine (1.83 g; 10.0 mmol) were dissolved in absolute ethanol (25 mL) and stirred overnight at 70° C. The solution was evaporated and crude ethyl 3-(diphenylmethylamino)propionate (2.85 g; 10.0 mmol) was dissolved in DMF (50 mL). 4-Methoxybenzenesulfonyl chloride (2.30 g; 11.0 mmol) and pyridine (10 mL) were added and the mixture stirred overnight at 70° C. The dark reaction was washed with 1 N HCl (2×100 mL). The combined extracts were washed with saturated aqueous NaCl (100 mL), dried over MgSO4, filtered, and evaporated to an oil. The black residue was eluted through a filter pad of silica gel using a hexanes/ethyl acetate step gradient to remove polar material. Preparative HPLC purification, eluting with a mixture of ethyl acetate/hexanes (35:65), gave 1.06 g (23%) of the title compound as a pale yellow oil. 300 MHz 1H-NMR (CDCl3): δ 1.16 (t, 3H), 2.12 (m, 2H), 3.57 (m, 2H), 3.84 (s, 3H), 3.99 (q, 2H), 6.48 (s, 1H), 6.83 (d, 2H), 7.04 (m, 4H), 7.24 (m, 6H), 7.64 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06506936B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-bbd7ca22e7dd4f52955dd5816b9e6b00 |
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| Source note | uspto-grants-2003_01 |
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