참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetone | HCID 180 | — |
| 반응물 | 4-Hydroxyisophthalic acid | HCID 12490 | — |
| 용매 | Trifluoroacetic acid | HCID 6422 | — |
| 용매 | Trifluoroacetic anhydride | HCID 9845 | — |
| 생성물 | 2,2-dimethyl-4-oxo-4H-1,3-benzodioxine-6-carboxylic acid | HCID 57554489 | 77% |
반응 단계
A suspension of 4-hydroxyisophtalic acid (Aldrich, 5.0 g, 27.5 mmol) in acetone (10 mL), TFA (30 mL) and TFAA (10 mL) was heated at 100° C. for 24 hrs. The reaction mixture was concentrated under reduced pressure. The residue was taken up with an aqueous solution of HCl (100 mL, 1N) and extracted with EtOAc (3×200 L); The combined organic layers were dried over MgSO4 and the solvents were removed under reduced: pressure. The crude compound was recrystallized in Et2O (50 mL) to give 4.67 g (77%) of the title compound as a beige powder. 1H NMR (DMSO-d6) δ: 8.37 (d J=1.9 Hz, 1H), 8.19 (dd, J=2.2 and 8.7 Hz, 1H), 7.23 (d, J=8.3 Hz, 1H), 1.72 (s, 6H). HPLC, Rt: 2.40 min (purity: 95.7%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07947851B2 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
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| ORD ID | ord-5239bc217de14bc19f5e1c209b28bbc8 |
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| 출처 메모 | uspto-grants-2011_05 |
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