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Norbornadiene → HCID 59749439, 화합물

HRID 747185
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인쇄 미리보기

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HRID 747185 반응식
[N:1]([CH2:4][CH:5]1[O:9][N:8]=[C:7]([C:10]2[CH:15]=[CH:14][C:13]([Br:16])=[CH:12][CH:11]=2)[CH2:6]1)=[N+:2]=[N-:3].[CH:17]12CC(C=C1)C=[CH:18]2>O1CCOCC1>[Br:16][C:13]1[CH:14]=[CH:15][C:10]([C:7]2[CH2:6][CH:5]([CH2:4][N:1]3[CH:18]=[CH:17][N:3]=[N:2]3)[O:9][N:8]=2)=[CH:11][CH:12]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8473NorbornadieneHCID 179544685-Azidomethyl-3-(4-bromo-phenyl)-4,5-dihydro-isoxazole

생성물 1

HCID 59749439HCID 59749439, 화합물수율 65.7%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

반응 조건

온도
100 °C

실험 절차

5-Azidomethyl-3-(4-bromo-phenyl)-4,5-dihydro-isoxazol (12.3 g, 43.6 mmol) and bicyclo[2.2.1]hepta-2,5-diene (23.6 ml, 218.1 mmol) were added to dioxane (200 ml), heated to 100° C. and stirred for six hours. The reaction mixture was concentrated in vacuo followed by addition of ethyl ether (200 ml). The precipitate was collected and washed with ethyl ether (3×20 ml) and dried under nitrogen to give the desired product (8.8 g).

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. additionfollowed by addition of ethyl ether (200 ml)
  3. customThe precipitate was collected
  4. washwashed with ethyl ether (3×20 ml)
  5. customdried under nitrogen

출처 및 근거

ORD 기록
ord-3e50b0ba231a47a58d07fc81d02524df
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07396847B2

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