関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydroquinone | HCID 785 | — |
| 反応物 | Maleic Anhydride | HCID 7923 | — |
| 反応物 | 1,3-Pentadiene | HCID 62204 | — |
| 反応物 | 1,3-Pentadiene, (3Z)- | HCID 643785 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4-Methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione | HCID 12726603 | 99% |
反応手順
Maleic anhydride (68.6 parts) and 70 parts of toluene were introduced into a pressure autoclave, and melted at 55° C. Then, 0.162 part of hydroquinone was added, and 130.9 parts (corresponding to 1.1 moles of trans-1,3-pentadiene per mole of maleic anhydride) of crude trans-1,3-pentadiene composed of 40 % of trans-1,3-pentadiene, 20 % of cis-1,3-pentadiene and 40 % of pentanes was continuously added over 6 hours at 50° C. The temperature was then raised to 60° C., and the reaction was carried out for 3 hours. After the reaction, the reaction mixture was distilled at 90° C. under atmospheric pressure to remove volatile components to give 3-methyltetrahydrophthalic anhydride (melting point 61° C.) in a yield of 99 % as a Diels-Alder reaction product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05019599 |
|---|
| 出典データセット | uspto-grants-1991_05 |
|---|
| ORD ID | ord-61db99f76e62470e820b5e99396eddbf |
|---|
| 出典メモ | uspto-grants-1991_05 |
|---|