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Acetic Acid → 4-((3,5-Bis(trifluoromethyl)benzyloxy)methyl)-1-ethyl-4-phenylazepane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 4-((3,5-Bis(trifluoromethyl)benzyloxy)methyl)-4-phenylazepane | HCID 11626160 | — |
| 生成物 | 4-((3,5-Bis(trifluoromethyl)benzyloxy)methyl)-1-ethyl-4-phenylazepane | HCID 21973113 | 56% |
反応手順
Isomer A of 4-((3,5-bis(trifluoromethyl)benzyloxy)methyl)-4-phenylazepane (3 mg), in glacial acetic acid (0.05 mL) was added sodium borohydride (2 mg) in two portions. After addition, the mixture was stirred at room temperature for overnight. The mixture was concentrated under vacuum. Then saturated sodium bicarbonate and dichloromethane was added to the mixture and the organic layer was separated. The aqueous layer was extracted with dichloromethane 2 times and the combined organic layers were dried over magnesium sulfate, filtered and concentrated under vacuum to give the product as a clear colorless sticky oil (1.8 mg, 56% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07098203B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-2a45246cc5f84d0cb90ea4bcf20c2b8c |
| 出典メモ | uspto-grants-2006_08 |