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1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 118023486, 화합물

HRID 1497008
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HRID 1497008 반응식
[CH2:1](O)/[CH:2]=[CH:3]/[CH:4]=[CH:5]/[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10]CC.C1(P([N:28]=[N+:29]=[N-:30])(C2C=CC=CC=2)=O)C=CC=CC=1.C1CCN2C(=NCCC2)CC1>C1(C)C=CC=CC=1>[N:28]([CH2:1]/[CH:2]=[CH:3]/[CH:4]=[CH:5]/[CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])=[N+:29]=[N-:30]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 199401P,P-Diphenylphosphinic azideHCID 64364912,4-Dodecadien-1-ol, (2E,4E)-

생성물 1

HCID 118023486HCID 118023486, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

(2E,4E)-Dodeca-2,4-dien-1-ol (4.95 g) was dissolved in dry toluene (110 ml) and diphenylphosphinyl azide (7.92 g) was added. DBU (4.91 ml) was added dropwise. The mixture turned opaque under evolution of heat. The solvent was evaporated and diethyl ether was added to the residue. The reaction mixture was washed with 1M HCl, 1M NaOH and brine and the organic layer was dried over sodium sulfate, filtered and concentrated to give a light yellow liquid. The crude product was filtered over silica gel.

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후처리

  1. temperatureof heat
  2. customThe solvent was evaporated
  3. additiondiethyl ether was added to the residue
  4. washThe reaction mixture was washed with 1M HCl, 1M NaOH and brine
  5. dry with materialthe organic layer was dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto give a light yellow liquid
  9. filtrationThe crude product was filtered over silica gel

출처 및 근거

ORD 기록
ord-b0107944063d4cbeb3bd51ff3aa6bcb9
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09199948B2

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