참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 3,4-Dimethoxy-5-hydroxybenzaldehyde | HCID 141513 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 2-(Mercaptomethyl)benzenethiol | HCID 5255139 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-(4H-benzo[d][1,3]dithiin-2-yl)-2,3-dimethoxyphenol | HCID 57750889 | 79.1% |
반응 단계
Hydrogen chloride gas was bubbled for three minutes at 22° C. through a solution of 3-hydroxy-4,5-dimethoxybenzaldehyde (0.55 g, 3.0 mmol) and 2-(mercaptomethyl)benzenethiol (0.52 g, 3.3 mmol) in dichloromethane (15 ml). After an additional 15 min., the reaction mixture was poured into saturated NaHCO3 (50 ml) and extracted with dichloromethane (2×75 ml). The combined organic layer was washed with brine (30 ml), dried (Na2SO4), filtered and concentrated providing a crude solid. This solid was triturated with hexane and then purified by flash chromatography using a gradient of hexanes (100%) up to hexanes (70%:30%). Concentration of the product containing fractions provided the above subtitle compound (0.76 g, 78%) as a white solid. 1H NMR (300 MHz, CDCl3, ppm) δ 3.84 (s, 3H), 3.90 (s, 3H), 3.94 (d, J=15 Hz, 1H), 4.00 (d, J=15 Hz, 1H), 5.42 (s, 1H), 5.89 (br s, 1H), 6.63 (d, J=2 Hz, 1H), 6.78 (d, J=2 Hz, 1H), 7.15-7.36 (m, 4H); 13C NMR (75 MHz, CDCl3, ppm) δ 34.3, 51.5, 56.0, 61.0, 104.1, 108.2, 126.4, 127.7, 128.5, 129.6, 135.2, 135.3, 135.5, 135.7, 149.4, 152.5; MS calculated for C16H16O3S2-H 319 observed 319.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08309598B2 |
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| 출처 데이터셋 | uspto-grants-2012_11 |
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| ORD ID | ord-6af6b7c3ef5b43e0abfdf6622caf7500 |
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| 출처 메모 | uspto-grants-2012_11 |
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