참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Dibenzofuranol | HCID 66587 | — |
| 반응물 | 3,4-dibenzyloxy-5-(2-hydroxyethyl)-2(5H)-furanone | HCID 21184106 | — |
| 생성물 | 5-[2-(dibenzofuran-2-oxy)ethyl]-3,4-dihydroxy-2(5H)-furanone | HCID 69941460 | 12.3% |
반응 단계
Mitsunoble coupling of 0.22 g (1.2 mmol) of 2-hydroxydibenzofuran with 0.34 g (1.0 mmol) of 3,4-dibenzyloxy-5-(2-hydroxyethyl)-2(5H)-furanone and subsequent benzyl group deprotection by hydrogenation were performed in a similar manner as described in the synthesis of 3,4-dihydroxy-5-[2-(4-phenoxy)phenoxyethyl]-2(5H)-furanone to provide 40 mg (10% yield) of 5-[2-(dibenzofuran-2-oxy)ethyl]-3,4-dihydroxy-2(5H)-furanone a white solid.: mp 191-192° C. (ether/hexanes), 1H NMR (acetone-d6) δ 8.23-8.18 (m, 1H), 7.83-7.44 (m, 5H), 7.28-7.23 (m, 1H), 5.12 (dd, J=5.3, 8.7 Hz, 1H), 4.42 (dd, J=2.6, 4.7 Hz, 2H), 2.69-2.59 (m, 1H), 2.21-2.08 (m, 1H). 13C NMR (acetone-d6) δ 169.68, 157.31, 155.75, 153.70, 151.31, 127.76, 125.05, 124.83, 123.07, 121.34, 118.46, 116.42, 112.39, 111.90, 105.40, 72.72, 64.57, 32.64. Anal Calcd for C18H14O6 +0.25 H2O: C, 65.36; H, 4.57. Found: C, 65.52; H, 4.23.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06136832 |
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| 출처 데이터셋 | uspto-grants-2000_10 |
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| ORD ID | ord-21caa20e277d41208181557179468cdd |
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| 출처 메모 | uspto-grants-2000_10 |
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