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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

반응식

참여 물질

역할이름HCID투입량
반응물Pivaloyl chlorideHCID 62493—
반응물Sodium BicarbonateHCID 516892—
반응물N-(2-phenylethyl)but-3-en-1-amineHCID 16720109—
반응물1-(1-Naphthalen-1-yl-ethyl)-aziridine-2-carboxylic acid methyl esterHCID 86601081—
반응물HCID 178504318HCID 178504318—
용매TetrahydrofuranHCID 8028—
생성물1-(1-Naphthalen-1-yl-ethyl)-aziridine-2-carboxylic acid but-3-enyl-phenethyl-amideHCID 8660108276.4%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419975B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-4b4676d8f0c54914b0b770a60ef616ca
출처 메모uspto-grants-2008_09