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Ammonia → 2-Butenoic acid, 3-amino-, 1-methylethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Isopropyl acetoacetate | HCID 68329 | — |
| 反応物 | 2,2,6-Trimethyl-4H-1,3-dioxin-4-one | HCID 79368 | — |
| 反応物 | 2-Methoxyethyl acetoacetate | HCID 89734 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 溶媒 | 2-Methoxyethanol | HCID 8019 | — |
| 生成物 | 2-Butenoic acid, 3-amino-, 1-methylethyl ester | HCID 11137274 | — |
反応手順
The ester, 2-methoxyethyl acetoacetate (51), was prepared by the reaction of 2-methoxyethanol with 2,2,6-trimethyl-4H-1,3-dioxin-4-one (53) (eq. 28). (Hyatt, J. A. J. Org. Chem. 1984, 49, 5102. Hyatt, J. A.; Feldman, P. L.; Clemens, R. J. Ibid. 1984, 49, 5105. Kato, T.; Sato, M.; Kanuma, N. Chem. Pharm. Bull. 1982, 30, 1315). The enamine, 1-methylethyl 3-aminocrotonate (52) was prepared by the reaction of ammonia with 1-methylethyl acetoacetate (54) (eq. 29) (Iwanami, J. et al. Chem. Pharm. Bull. 27, 1426 (1979)) which was obtained by the reaction of 2-propanol with 53 (eq. 30) as shown in Schemes IIa, IIb and IIc. ##STR13##
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04758669 |
| 出典データセット | uspto-grants-1988_07 |
| ORD ID | ord-87eac25bdedb47f8b405a5a9914badb7 |
| 出典メモ | uspto-grants-1988_07 |