性质与稳定性:在常温和常压条件下,不会发生分解反应。
化学性质
α-甲基乙酰乙酸乙酯纯品为无色透明液体,具有酯的香味,熔点为-45℃,沸点188℃,折射率(nD20) 1.4182,相对密度1.0190。该物质易溶于苯和二甲苯,而不溶于水。
用途
α-甲基乙酰乙酸乙酯主要用于制备农药抗蚜威的中间体,并作为医药及农药的重要中间体。
生产方法
α-甲基乙酰乙酸乙酯可以通过乙酰乙酸乙酯与硫酸二甲酯反应制得。具体操作如下:在搪玻璃反应釜中预先加入二甲苯、乙酰乙酸乙酯、硫酸二甲酯和相转移催化剂,搅拌均匀后缓缓加入氢氧化钠溶液,确保反应温度不超过40℃。继续搅拌1.5小时,控制pH值为8~9,然后静置1小时。分出水层,并用水洗至水溶液呈中性。静置后再次分离水层并送入三废处理系统。二甲苯溶液在减压下脱水浓缩,直至乳状α-甲基乙酰乙酸乙酯的含量达到35%~40%,即可停止浓缩,得到乳状α-甲基乙酰乙酸乙酯二甲苯溶液,最后进行脱溶以获得产品。
| 中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
|---|---|---|---|---|
| 2-甲酰基-3-氧代丁酸乙酯 | 2-formyl-3-oxo-butyric acid ethyl ester | 33142-24-4 | C7H10O4 | 158.154 |
| 乙酰乙酸乙酯 | ethyl acetoacetate | 141-97-9 | C6H10O3 | 130.144 |
| —— | 2-hydroxymethyl-2-methyl-acetoacetic acid ethyl ester | 82515-48-8 | C8H14O4 | 174.197 |
| 2-氧代环戊羧酸乙酯 | 2-ethoxycarbonyl-1-cyclopentanone | 611-10-9 | C8H12O3 | 156.181 |
| 3-羟基-2-甲基丁酸 | ethyl 3-hydroxy-2-methylbutyrate | 27372-03-8 | C7H14O3 | 146.186 |
| 中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
|---|---|---|---|---|
| —— | butyl 2-methyl-3-oxobutanoate | 126045-59-8 | C9H16O3 | 172.224 |
| —— | ethanoylpropanoic acid isobutyl ester | 104061-13-4 | C9H16O3 | 172.224 |
| —— | Neopentyl 2-methyl-3-oxobutanoate | 137998-56-2 | C10H18O3 | 186.251 |
| —— | isopropyl 2-methyl-3-oxobutanoate | 919771-62-3 | C8H14O3 | 158.197 |
| —— | ethanoylpropanoic acid-n-hexyl ester | 94723-90-7 | C11H20O3 | 200.278 |
| —— | Allyl 2-methyl-3-oxobutanoate | 111903-66-3 | C8H12O3 | 156.181 |
| 2-甲基-3-氧代丁酸辛酯 | octyl 2-methyl-3-oxobutanoate | 104061-14-5 | C13H24O3 | 228.332 |
| 2-甲基-3-氧代丁酸甲酯 | 2-methyl-acetoacetic acid methyl ester | 17094-21-2 | C6H10O3 | 130.144 |
| —— | (E)-2-butenyl 2-methyl-3-oxobutanoate | 111903-67-4 | C9H14O3 | 170.208 |
| —— | 2-Butoxyethyl 2-methyl-3-oxobutanoate | 137998-57-3 | C11H20O4 | 216.277 |
| 2-甲基-3-氧代丁酸叔丁酯 | tert-butyl 2-methyl-3-oxobutanoate | 39149-65-0 | C9H16O3 | 172.224 |
| 2,2-二甲基-3-氧代丁酸乙酯 | ethyl 2,2-dimethyl-3-oxobutanoate | 597-04-6 | C8H14O3 | 158.197 |
| —— | (R)-ethyl 2-methyl-3-oxopentanoate | 138752-69-9 | C8H14O3 | 158.197 |
| —— | 3-methyl-2-butenyl 2-methyl-3-oxobutanoate | 111903-68-5 | C10H16O3 | 184.235 |
| 4-溴-2-甲基-3-氧代丁酸乙酯 | ethyl 4-bromo-2-methyl-3-oxobutanoate | 51461-34-8 | C7H11BrO3 | 223.067 |
| —— | 1-methyl-2-propenyl 2-methyl-3-oxobutanoate | 111903-69-6 | C9H14O3 | 170.208 |
| 2-甲基-3-氧代己酸乙酯 | 2-methyl-3-oxo-hexanoic acid ethyl ester | 29304-40-3 | C9H16O3 | 172.224 |
| —— | (Z)-3-methyl-2-pentenyl 2-methyl-3-oxobutanoate | 122305-25-3 | C11H18O3 | 198.262 |
| 2-乙基-2-甲基乙酰乙酸乙酯 | ethyl 2-ethyl-2-methylacetoacetate | 33697-53-9 | C9H16O3 | 172.224 |
| —— | ethyl 2-methyl-3-oxoheptanoate | 2866-79-7 | C10H18O3 | 186.251 |
| —— | 2,5-dimethyl-3-oxohexanoic acid ethyl ester | 10488-92-3 | C10H18O3 | 186.251 |
| —— | ethyl 2-methyl-3-oxooctanoate | 10488-94-5 | C11H20O3 | 200.278 |
| —— | ethyl 2-methyl-3-oxo-nonanoate | 2867-60-9 | C12H22O3 | 214.305 |
| 2-甲基-3-氧代癸酸乙酯 | ethyl 2-methyl-3-oxodecanoate | 100545-22-0 | C13H24O3 |