Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29056생성일: 2026년 10월 25일
Pivaloyl chloride → 1-(1-Naphthalen-1-yl-ethyl)-aziridine-2-carboxylic acid but-3-enyl-phenethyl-amide
https://huagongshe.com/reaction/29056
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pivaloyl chloride | HCID 62493 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | N-(2-phenylethyl)but-3-en-1-amine | HCID 16720109 | — |
| 반응물 | 1-(1-Naphthalen-1-yl-ethyl)-aziridine-2-carboxylic acid methyl ester | HCID 86601081 | — |
| 반응물 | HCID 178504318 | HCID 178504318 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(1-Naphthalen-1-yl-ethyl)-aziridine-2-carboxylic acid but-3-enyl-phenethyl-amide | HCID 86601082 | 76.4% |
반응 단계
To a solution of 1 (12.6 g, 49.75 mmol) in THF (200 mL) is added KOTMS (6.38 g, 49.75 mmol). The mixture is stirred overnight at room temperature. The mixture is concentrated and the residue dissolved in dichloromethane (200 mL) and cooled to 0° C. Trimethylacetyl chloride (5.94 g, 49.25 mmol) is added slowly and the mixture is warmed to room temperature over 2 hours. The mixture is cooled to −78° C., 2 (8.63 g, 49.25 mmol) is added and stirring continued at −78° C. for 1.5 h. Saturated sodium bicarbonate (100 mL) is added and the mixture is allowed to warm to rt. The mixture is extracted with EtOAc (4×100 mL) and the organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 15 g (76%) of the title compound as a mixture of two diastereomers in an equimolecular ratio. M+H+=399.37.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07419975B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-4b4676d8f0c54914b0b770a60ef616ca |
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| 출처 메모 | uspto-grants-2008_09 |
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