참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phthalic Anhydride | HCID 6811 | — |
| 반응물 | 2-Methylresorcinol | HCID 11843 | — |
| 반응물 | Aluminum(III) Chloride | HCID 6451240 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | 1,1,1,2-Tetrachloroethane | HCID 12418 | — |
| 생성물 | 2-(2,4-Dihydroxy-3-methylbenzoyl)benzoic acid | HCID 21083111 | — |
반응 단계
Aluminum chloride (21.4 g, 161 mmol) was added to a stirring suspension of phthalic anhydride (6 g, 40 mmol) in tetrachloroethane (200 mL) under nitrogen. 1,3-Dihydroxy-2-methylbenzene (5 g, 40 mmol) was added and the mixture quickly thickened. After the precipitates were broken up with a spatula the reaction continued for 1 hour. The solution was diluted with ethyl acetate (˜600 mL) and washed with 1 M hydrochloric acid (2×200 mL). The product was extracted from the organic layer into a saturated solution of sodium bicarbonate in water (600 mL). The basic aqueous phase was acidified with 3M hydrochloric acid to a pH of 5. The product was extracted from the aqueous phase into ethyl acetate (400 mL), washed with brine (2×100 mL), dried over magnesium sulfate and concentrated to give a brownish solid. The solid was slurried in dichloromethane (20 mL) and filtered to give 2-(2,4-dihydroxy-3-methylbenzoyl)benzoic acid as an off white powder (4.6 g, 16.9 mmol, 42% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07504360B2 |
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| 출처 데이터셋 | uspto-grants-2009_03 |
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| ORD ID | ord-4d55731c11f64cea9f07bcf59e7d1826 |
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| 출처 메모 | uspto-grants-2009_03 |
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