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

HRID 561251
ノート
印刷プレビュー

反応式

HRID 561251 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-7e35a3e2ba2e41e188a3492ce7ecf64c
出典データセット
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08063231B2

反応ノート

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