Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10177생성일: 2026년 10월 23일
N,N,N',N'-Tetramethylethylenediamine → 4-Benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/ko/reaction/10177
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 반응물 | 2-Bromomethylnaphthalene | HCID 70320 | — |
| 반응물 | Tert-butyl 4-benzylpiperazine-1-carboxylate | HCID 584330 | — |
| 반응물 | CID 53628100 | HCID 178418400 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 4-Benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl ester | HCID 21041081 | — |
반응 단계
To a solution of 4-benzyl-piperazine-1-carboxylic acid tert-butyl ester (2 g) in diethylether (35 mL) was added tetramethylethylenediamine (1.4 mL). The resulting mixture was cooled to −70° C. and sec-butyllithium (7 mL of a 1.3 M solution) was added dropwise, after complete addition the solution was slowly warmed to −10° C., at which temperature the mixture was stirred for one hour. Subsequently, the mixture was recooled to −70° C.; then a solution of 2-(bromomethyl)naphthalene (2 g) in diethylether was added dropwise and stirring continued at −70° C. was continued for one hour. The resulting mixture was stirred and allowed to come to room temperature overnight, then partitioned between saturated ammonium chloride (aq) and ethyl acetate. The organic layer was dried over magnesium sulphate, filtered, and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, CH2Cl2/MeOH 99/1) to afford 4-benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl ester as an oil. 0.8 g (27 %) Rf 0.47 (CH2Cl2/MeOH 99/1), MH+ 417.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07094779B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-4894c875297347dab46acb76b5f533c2 |
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| 출처 메모 | uspto-grants-2006_08 |
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