참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | 3-Bromo-4-methylbenzoic acid | HCID 82130 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 반응물 | HCID 178418689 | HCID 178418689 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Methylbenzene-1,3-dicarboxylic acid | HCID 595750 | — |
반응 단계
To THF (130 ml) solution of 3-bromo-4-methyl-benzoic acid (5.0 g, 23.25 mmol) under nitrogen and cooled to −78° C. (dryice/methanol) was added MeMgBr in ether (3.0 M, 8.5 ml, 25.57 mmol) at such a rate that the temperature did not exceed −75° C. The temperature was then allowed to rise to −60° C. and after gas evolution had ceased, the solution was cooled again to −78° C. BuLi in hexane (1.6 M, 29.06 ml, 46.50 mmol) was then added dropwise such that the temperature did not rise above −75° C. The mixture was then stirred at this temperature for 15 minutes before crushed dryice (4.4 g, 100 mmol) was added. The precipitate was vigorously stirred as the temperature was allowed to freely rise to ambient temperature. The mixture was made acidic using 6 N HCl and the solid material collected filteration, washed with diethyl ether and dried. Recrystallisation from water afforded off-white pure compound (81%) m.p. 296-298° C. (sublimed). NMR conforms to expected structure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06610269B1 |
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| 출처 데이터셋 | uspto-grants-2003_08 |
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| ORD ID | ord-5f555154eb014f07a1c4fbee0b2d32dc |
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| 출처 메모 | uspto-grants-2003_08 |
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