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HRID 2175778作成日:2026年10月25日
4-bromo-N,N-diethyl-2-[(2R)-2-hydroxypropyl]benzamide → (3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-one
https://huagongshe.com/reaction/2175778
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 4-bromo-N,N-diethyl-2-[(2R)-2-hydroxypropyl]benzamide | HCID 86693033 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | (3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-one | HCID 71270763 | — |
反応手順
A solution of 4-bromo-N,N-diethyl-2-[(2R)-2-hydroxypropyl]benzamide (12.2 g, 38.8 mmol) dissolved in 4N HCl in dioxane (200 mL) was stirred at room temperature and monitored by TLC. After 3 days the reaction was partitioned between EtOAc (300 mL) and water (300 mL). The aqueous phase was further extracted with EtOAc (2×250 mL). The combined organic layers were then washed with water (200 mL), brine (200 mL), dried over magnesium sulfate, filtered and concentrated. The crude material was then purified via MPLC (15-30% EtOAc/Hexane) to afford (3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-one: 1H NMR (500 MHz; CDCl3): 7.98 (d, J=8.2 Hz, 1H), 7.56 (dd, J=1.5, 8.2 Hz, 1H), 7.45 (s, 1H), 4.71 (m, 1H), 2.94 (m, 2H), 1.55 (d, J=6.3 Hz, 3H); LC-MS: (M+1)+ 241.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09062070B2 |
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| 出典データセット | uspto-grants-2015_06 |
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| ORD ID | ord-10d94f4369b243c4a4a984d2df7137e7 |
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| 出典メモ | uspto-grants-2015_06 |
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