참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lead tetraacetate | HCID 11025 | — |
| 반응물 | Perchloric Acid | HCID 24247 | — |
| 반응물 | Ethyl orthoformate | HCID 31214 | — |
| 반응물 | 4-Propanoylanisole | HCID 67144 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Potassium Hydroxide | HCID 14797 | — |
| 생성물 | p-Methoxyphenylpropionic acid | HCID 257576 | 63.5% |
반응 단계
A mixture of p-methoxypropiophenone (2.39 g, 14.5 mmol), 90% lead(IV)acetate (6.45 g, 14.5 mmol), triethylorthoformate (15 ml) and 70% perchloric acid (1.2 ml. 29 mmol) was heated to 55° C. for 18 h. The mixture was cooled and the triethylorthoformate removed under reduced pressure. The residue was dissolved in CHCl3 and the remaining precipitate filtered off and discarded. The CHCl3 solution was then washed with water and evaporated to yield the crude ester. This crude ester product was dissolved in a 10% KOH 1:1 water:methanol solution, which was then refluxed for 3 h. After cooling the methanol was evaporated under reduced pressure and the aqueous solution washed with diethylether (3×25 ml). The aqueous solution was acidified with 2N H2SO4, then washed again with diethylether (3×25 ml). The combined fractions from the second ether wash were dried (Na2SO4) and evaporated to give the propionic acid (1.66 g, 63%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07419998B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-296cb2a7bea74433a90a47142849b1ea |
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| 출처 메모 | uspto-grants-2008_09 |
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