참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | 4-Aminophenylacetic acid | HCID 14533 | — |
| 반응물 | 2-(4-Aminophenyl)acetamide | HCID 238034 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | HCID 85804887 | HCID 85804887 | 80% |
반응 단계
The 4-aminophenylacetamide used in this example was obtained according to patent literature WO 02/08247 A2 or WO 03/051909 A2. Procedure was as follows: Methanol (200 mL) was charged to 4-aminophenylacetic acid (Aldrich) (25 g, 0.165 mol). Sulfuric acid (18 mL concentrated, 0.648 mol) was added maintaining the temperature <20° C. The mixture was then refluxed for one hour and concentrated by distillation at atmospheric pressure until the volume of 140 mL. The mixture was then cooled to 50° C. and tert-buthyl methyl ether (300 mL) was added maintaining the temperature above 45° C. The mixture was gradually cooled to 0-5° C. and held at this temperature for 1 hour. The resultant crystalline product was isolated by filtration and washed with cold methanol:tert-butyl methyl ether (20 mL:55 mL) and cold tert-butyl methyl ether and then dried under vacuum to give methyl 4-aminophenylacetate hydrogensulfate (35.3 g, 80% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08487130B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-af354de492ca4915871b09f55db1b9e0 |
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| 출처 메모 | uspto-grants-2013_07 |
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