関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrogen Bromide | HCID 260 | — |
| 反応物 | 2-(4-Amino-3-chloro-5-trifluoromethylphenyl)-2-tert-butylaminoethanol | HCID 9997789 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 2-(4-Amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylamino-ethanol hydrobromide | HCID 21977096 | 80% |
反応手順
1.0 g of 2-(3-chloro-4-amino-5-trifluoromethyl-phenyl)-2-tert-butylaminoethanol was dissolved in 20 ml of anhydrous diethyl ether and the solution was acidified to pH=2 by adding dropwise a solution of hydrobromic acid in isopropanol with stirring. The precipitate was collected by filtration, washed with small amount of anhydrous diethyl ether, dried to give crude 2-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylamino-ethanol hydrobromide. The crude product was dissolved in absolute ethanol at a ratio of 1:5 w/v. Filtered and anhydrous diethyl ether was added dropwise until small amount of crystals was precipitated. Lyophilized and filtered to give 2-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylamino-ethanol hydrobromide. Yield 80–90%; melting point 208–210° C. (dec). 1H-NMR (DMSO-d6) δ: 1.24(9H, s), 3.79(2H, d), 4.46–4.51(1H, m), 7.72(1H, s), 7.89(1H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07098364B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-484020b3048d494b90cf506b9fcdd076 |
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| 出典メモ | uspto-grants-2006_08 |
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