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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1097628생성일: 2026년 10월 26일

Hexamethylphosphoramide → 2-(3-Nitro-3-phenyl-propyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1097628

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylphosphoramideHCID 12679—
반응물(Nitromethyl)benzeneHCID 69321—
반응물Tert-butyl 2-(2-bromoethyl)pyrrolidine-1-carboxylateHCID 57850131—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물2-(3-Nitro-3-phenyl-propyl)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 58567897—

반응 조건

온도-2 °C

반응 단계

To a −78° C. solution of 200 mg (1.460 mmol) 2-(2-bromo-ethyl)-pyrrolidine-1-car boxylic acid tert-butyl ester (CAS: 958026-65-8) in 4.3 ml tetrahydrofuran over mol-sieves and 851.0 ul HMPA, was added drop-wise 1.92 ml (3.064 mmol) n-BuLi (1.6 M in hexane). After 45 minutes at −78° C., a solution of 406.2 mg (1.460 mmol) nitromethyl-benzene in 0.6 ml tetrahydrofuran over mol-sieves was added drop-wise. After 1 hour at −78° C., the reaction mixture was allowed to warm up slowly (during 5 hours) to −2° C. The mixture was then cooled again to −78° C. and quenched at this temperature with 0.4 ml of acetic acid, then with 8 ml saturated ammonium chloride. Back to room temperature, the aqueous phase was extracted 2 times with ethylacetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude yellow oil (993 mg) was purified with flash column chromatography on silica eluting from n-heptane and ethyl acetate (0 to 15%) to provide 242 mg (y: 49.6%) of the title compound as a colorless oil. MS (m/e): 335.2 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143273B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-cf5d6be4c99641e1911a31bd03512c19
출처 메모uspto-grants-2012_03