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1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-(Azidomethyl)-3-bromo-2-methoxybenzene

HRID 574736
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HRID 574736 반응식
P([N:17]=[N+:18]=[N-:19])(=O)(OC1C=CC=CC=1)OC1C=CC=CC=1.N12CCCN=C1CCCCC2.[Br:31][C:32]1[C:33]([O:40][CH3:41])=[C:34]([CH2:38]O)[CH:35]=[CH:36][CH:37]=1>C1(C)C=CC=CC=1>[N:17]([CH2:38][C:34]1[CH:35]=[CH:36][CH:37]=[C:32]([Br:31])[C:33]=1[O:40][CH3:41])=[N+:18]=[N-:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 123414Diphenylphosphoryl azideHCID 177503163-Bromo-2-methoxybenzenemethanol

생성물 1

HCID 597786811-(Azidomethyl)-3-bromo-2-methoxybenzene

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

6.00 g of diphenyl phosphorazidate and 4.1 g of 1,8-diazabicyclo[5.4.0]undec-7-ene were added to 4.0 g of 3-bromo-2-methoxy-phenyl-methanol 6 in 100 mL of toluene at 0° C. The mixture was stirred at room temperature overnight. The reaction mixture was quenched with aqueous ammonium chloride. The aqueous layer was extracted with ethyl acetate/THF. The pooled organic extracts were washed with brine and dried over magnesium sulfate. The mixture was filtered. The solvents were removed under vacuum. The residue was purified by chromatography on silica gel to give 1-azidomethyl-3-bromo-2-methoxy-benzene 7.

후처리

  1. customThe reaction mixture was quenched with aqueous ammonium chloride
  2. extractionThe aqueous layer was extracted with ethyl acetate/THF
  3. washThe pooled organic extracts were washed with brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationThe mixture was filtered
  6. customThe solvents were removed under vacuum
  7. customThe residue was purified by chromatography on silica gel

출처 및 근거

ORD 기록
ord-505c849f323a402e80798d500de0f63d
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09034910B2

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