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Acetaldehyde → Ethyl 2-ethylidene-4-chloro-3-oxobutyrate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetaldehyde | HCID 177 | — |
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | Ethyl 4-chloroacetoacetate | HCID 69484 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Ethyl 2-ethylidene-4-chloro-3-oxobutyrate | HCID 54518096 | — |
反応手順
0.25 part by weight of piperidine is added dropwise to a mixture of 32.9 parts by weight of ethyl 4-chloroacetoacetate and 9.6 parts by weight of acetaldehyde at -20° C. The mixture is left to stand at -20° C. for 5 to 6 hours and ice-cold 1N hydrochloric acid and ethyl acetate are then added. The ethyl acetate phase is separated off, extracted twice more with 1N hydrochloric acid and then once with water, dried over magnesium sulphate and concentrated. 35.6 parts by weight of a yellow oil are obtained, and are distilled using a bulb tube (oven temperature 80° to 110° C. under 0.07 mm). 15.5 parts by weight of product are obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04782162 |
| 出典データセット | uspto-grants-1988_11 |
| ORD ID | ord-e34ba31881ce473ead9df2b0d6453007 |
| 出典メモ | uspto-grants-1988_11 |