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Triethylamine → Methyl 3-ethoxy-2-(ethoxyimino)-3-iminopropanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Fluoride Ion | HCID 28179 | — |
| 反応物 | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| 反応物 | Methyl 3-amino-2-(ethoxyimino)-3-oxopropanoate | HCID 53690437 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Methyl 3-ethoxy-2-(ethoxyimino)-3-iminopropanoate | HCID 53663360 | — |
反応手順
To a solution of Meerwein reagent (triethyloxonium tetrafluoroborate) {prepared from bron fluoride etherate (2.84 g) by a method of Org. Syn., 46, 113 (1966)} in methylene chloride (30 ml) was added methyl 2-carbamoyl-2-ethoxyiminoacetate (syn isomer, 2.6 g) and the mixture was stirred for 18 hours at room temperature. The reaction mixture was cooled in an ice-bath and triethylamine (3 g) was added thereto, followed by an addition of water (20 ml). The organic layer was separated out, dried over magnesium sulfate and evaporated to give crude methyl 3-imino-3-ethoxy-2-ethoxyiminopropionate (syn isomer) (5.0 g) as an oil. ##STR15##
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04407798 |
| 出典データセット | uspto-grants-1983_10 |
| ORD ID | ord-c2c14045175f4522914e930aa28b5372 |
| 出典メモ | uspto-grants-1983_10 |