참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | 4-Chloro-3,5-dimethylphenol | HCID 2723 | — |
| 반응물 | Dimethyl acetylenedicarboxylate | HCID 12980 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 6-chloro-5,7-dimethyl-4-oxo-4H-1-benzopyran-2-carboxylic acid | HCID 21392596 | — |
반응 단계
0.5 Parts of benzyl trimethylammonium hydroxide were added dropwise to a mixture of 156.6 parts of 4-chloro-3, 5-xylenol, 149.1 parts of dimethyl acetylene dicarboxylate and 30 parts of dioxan. The reaction mixture was heated for 1/2 hour on the steam bath, cooled, and basified with 320 parts of 25% aqueous sodium hydroxide solution. After addition of 100 parts of methanol the red solution was heated at reflux for 3 hours on the steam bath, cooled, and acidified with excess dilute sulphuric acid. The precipitated yellow solid was filtered, washed with a little water, and dried. The solid was added portionwise to 850 parts of stirred chlorosulphonic acid cooled to 0° C. When all the solid had dissolved, the dark red solution was added cautiously dropwise to excess ice-water. The precipitated solid was filtered, washed with water, and recrystallised from a dioxan aqueous ethanol mixture to give 157.1 parts of 6-chloro-5,7-dimethyl-4-oxo-4H-1-benzopyran-2-carboxylic acid as a colourless solid, melting point 289°-290° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04064256 |
|---|
| 출처 데이터셋 | uspto-grants-1977_12 |
|---|
| ORD ID | ord-39b0c557d23b47318e7ee8c4f9597455 |
|---|
| 출처 메모 | uspto-grants-1977_12 |
|---|