돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3301생성일: 2026년 10월 24일

Phenyl isocyanate → 7a-(3-ethyl-5-isoxazolyl)-hexahydro-1H-pyrrolizine

https://huagongshe.com/ko/reaction/3301

반응식

참여 물질

역할이름HCID투입량
반응물Phenyl isocyanateHCID 7672—
반응물1-NitropropaneHCID 7903—
반응물7a-ethynylhexahydro-1H-pyrrolizineHCID 19597695—
용매BenzeneHCID 241—
생성물7a-(3-ethyl-5-isoxazolyl)-hexahydro-1H-pyrrolizineHCID 1893475150.1%

반응 단계

Nitropropane (0.475 mL, 5.29 mmol) and phenylisocyanate (1.0 mL, 9.5 mmol) were dissolved in benzene (10 mL) and added to a flask containing 7a-ethynyl-hexahydro-1H-pyrrolizine (358 mg, 2.65 mmol, from step 13a). The solution was stirred at ambient temperature for 1 hour and at reflux for 5 hours. The mixture was cooled, filtered, concentrated and diluted with EtOAc. The solution was extracted with 6N HCl. The aqueous phase was made basic with 15% NaOH and extracted with methylene chloride. The organic extracts were combined, dried (MgSO4) and concentrated. The residue was residue was chromatographed (silica gel; CHCl3 /MeOH, 98:2) to afford an amber oil (274 mg, 50%). 1H NMR (CDCl3, 300 MHz) δ1.25 (t, J=7.5 Hz, 3H), 1.75-1.92 (m, 6H), 2.15-2.25 (m, 2H), 2.60-2.69 (m, 4H), 3.13-3.20 (m, 2H), 5.98 (s, 1H); MS (CI/NH3) m/z: 207 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733912
출처 데이터셋uspto-grants-1998_03
ORD IDord-8757226fe4fa4085a41ed03eefc15d62
출처 메모uspto-grants-1998_03