참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 2-[4-(Dimethylamino)benzoyl]benzoic acid | HCID 88937 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | 3-Methoxy-3-(4-dimethylaminophenyl)phthalide | HCID 15918699 | — |
반응 단계
Following a procedure similar to that described in Example 1 above, 4.5 g of 2-(4-dimethylaminophenyl)carbonylbenzoic acid, 1.2 ml of thionyl chloride and 5.0 ml of methyl alcohol were interacted in 30.0 ml of ethylene dichloride in the presence of 1.3 ml of piperidine at ambient temperature for approximately ten minutes to obtain 4.0 g of 3-methoxy-3-(4-dimethylaminophenyl)phthalide (Formula II: R0 =R=R1 =R2 =R5 =H; R4 =R4' =R5Y=CH3 ; X=O), a pale peach-colored solid which melted at 112.5° to 114.5° C. A significant infrared maximum appeared at 1773 cm-1 (C=O; s). The nuclear magnetic resonance spectrum was consistent with the assigned structure. Analysis by mass spectrum showed m/e peaks at 283 (M+) and 252 (M+ -OCH3). A toluene solution of the product spotted on an acidic clay-coated paper developed a yellow-colored image.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04688059 |
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| 출처 데이터셋 | uspto-grants-1987_08 |
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| ORD ID | ord-8f2a46ac08b540f895adb954e2d1b4c0 |
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| 출처 메모 | uspto-grants-1987_08 |
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