참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | 4-[3-(Trifluoromethyl)phenyl]-4-piperidinol | HCID 75255 | — |
| 반응물 | Triphosgene | HCID 94429 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Hydroxy4-[3-(trifluoromethyl)phenyl]piperidine-1-carbonyl chloride | HCID 59011934 | 203.6% |
반응 단계
A solution of triphosgene (3.26 g, 0.011 mol) and anhydrous tetrahydrofuran (1000 mL) cooled to −20° C. was treated with pyridine (4.45 mL, 0.055 mol). The resulting cloudy suspension was slowly treated with a solution of 4-(3-trifluoromethyl-phenyl)-piperidin-4-ol (9 g, 0.036 mol) in anhydrous tetrahydrofuran (45 mL) while the internal temperature was maintained between −20° C. to −30° C. The resulting mixture was transferred to an ice bath which was allowed to come to 25° C. overnight to give a light brown solution with a small amount of brown precipitates. The reaction mixture was then concentrated in vacuo to give a brown solid. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 75/25 hexanes/ethyl acetate) afforded 4-hydroxy-4-(3-trifluoromethyl-phenyl)-piperidine-1-carbonyl chloride (6.89 g, 61%) as a clear, viscous oil. The NMR spectrum obtained on the sample is compatible with its structure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07947692B2 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
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| ORD ID | ord-124a997a12b24ae5aab50a5ad76a1a59 |
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| 출처 메모 | uspto-grants-2011_05 |
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