돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19353생성일: 2026년 10월 26일

1,8-Diazabicyclo(5.4.0)undec-7-ene → 2-Benzyloxycarbonylamino-3-bicyclo[2.2.1]hept-2-yl-acrylic acid methyl ester

https://huagongshe.com/reaction/19353

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Bicyclo[2.2.1]heptane-2-carbaldehydeHCID 86864—
반응물N-(benzyloxycarbonyl)-alpha-phosphonoglycine methyl esterHCID 66895383—
용매DichloromethaneHCID 6344—
생성물2-Benzyloxycarbonylamino-3-bicyclo[2.2.1]hept-2-yl-acrylic acid methyl esterHCID 6689557336.2%

반응 조건

온도0 °C

반응 단계

In a round bottom flask was placed N-(benzyloxycarbonyl)-α-phosphonoglycine methyl ester (2.05 g, 6.18 mmol) in dichloromethane (5 mL) and cooled to 0° C. in an ice bath. To this mixture was then added slowly 1,8-diazabicyclo[5.4.0]undec-7-ene (801 μL, 5.36 mmol) and it was stirred at 0° C. for 20 min. The mixture was then treated with a solution of bicyclo[2.2.1]heptane-2-carbaldehyde (512 mg, 4.12 mmol) in dichloromethane (5 mL). After the addition was complete, the mixture was allowed to warm to 25° C. and stirred overnight. The mixture was concentrated in vacuo and then dissolved in ethyl acetate (50 mL) and washed with a saturated aqueous ammonium chloride solution (2×25 mL). The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo. Purification by AnaLogix IntelliFlash chromatography (25 g column, 15% ethyl acetate/hexanes to 34% ethyl acetate/hexanes) afforded 2-benzyloxycarbonylamino-3-bicyclo[2.2.1]hept-2-yl-acrylic acid methyl ester (491 mg, 36%) as a clear colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741327B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f3903de789ea44f0b69e74904d176209
출처 메모uspto-grants-2010_06