Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | p-Chloroacetoacetanilide | HCID 7587 | — |
| Product | HCID 14128624 | HCID 14128624 | 77.5% |
Reaction Steps
A mixture of 2.12 g (10 m mol) of p-chloroacetoacetanilide, 1.07 g (10 m mol) of benzylamine and 20 ml of toluene was refluxed for 1 hour, while the resulted water together with about 12 ml of toluene were distilled off outside the reaction system. After the remaining solvent in the mixture was removed by a rotary evaporator under vacuo, 4.49 g (22 m mol) of 2,2-dimethyl-6-phenyl-4H-1,3-dioxin-4-one, 4.65 g (40 m mol) of N,N,N',N'-tetramethylethylenediamine and 20 ml of xylene were added to the residue. While further refluxing gently for 1.5 hours, the resulted acetone was removed to outside the reaction system. The mixture was cooled to precipitate the crystals. The crystals were filtered and dried to afford 2.63 g of the title compound (yield: 77.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04886546 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-d00000d9f3b745b6a8467c6d78e552d5 |
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| Source note | uspto-grants-1989_12 |
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