참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | 1,1-Dichloroethane | HCID 6365 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 5-Methylisophthalic acid | HCID 68137 | — |
| 촉매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | 3-(Methoxycarbonyl)-5-methylbenzoic acid | HCID 7210836 | — |
반응 단계
5-Methylisophthalic acid (1.21 g, 6.5 mmol), dichloroethane (20 mL), DMF (3 drops), and thionyl chloride (2.42 g, 20 mmol) was heated to 80° C. for 4 hrs. The reaction was concentrated to dryness and a solution of MeOH (208 mg, 6.5 mmol) was added slowly and the reaction was stirred overnight at rt. 1 N Hydrochloric acid (10 mL) was added and reaction stirred for 1 hr. The pH was adjusted with sat'd sodium bicarbonate (50 mL) and the aqueous solution was extracted with methylene chloride to remove the diester. The aqueous portion was then acidified with 1 N HCl and extracted with methylene chloride/MeOH 95:5. The organic extracts were dried over sodium sulfate, filtered, concentrated, and the product was isolated via preparative reverse-phase HPLC.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07985861B2 |
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| 출처 데이터셋 | uspto-grants-2011_07 |
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| ORD ID | ord-329a9160cac24fd3be89323743149f7a |
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| 출처 메모 | uspto-grants-2011_07 |
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