Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 634861생성일: 2026년 10월 25일
Acetone → N-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine
https://huagongshe.com/reaction/634861
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetone | HCID 180 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 5-(4-Bromomethylphenyl)-2-methyl-2H-tetrazole | HCID 589329 | — |
| 반응물 | 4-[Bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine | HCID 19040926 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine | HCID 15515185 | 32.9% |
반응 단계
This compound was prepared in a manner analogous to that of Step D of Example 4, with 0.3 gram (0.001 mole) of 4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl bromide, 0.5 gram (0.001 mole) of 4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine (prepared as in Step C of Example 4), and 0.6 gram (0.004 mole) of N,N-diisopropylethylamine in about 5 mL of dimethyl sulfoxide as reagents. The crude reaction product was subjected to column chromatography on silica gel, with 3:7 acetone:methylene chloride as the eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding about 0.2 gram of N-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine. The NMR spectrum was consistent with the proposed structure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06184234B2 |
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| 출처 데이터셋 | uspto-grants-2001_02 |
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| ORD ID | ord-e2fcd7fe246e4e6298eb9ecad3759803 |
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| 출처 메모 | uspto-grants-2001_02 |
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