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Sodium Azide → 2-Azidomethyl-3-phenylbenzo[b]thiophene

HRID 242859
ノート
印刷プレビュー

反応式

HRID 242859 の反応式
[N-:1]=[N+:2]=[N-:3].[Na+].[C:5]1([C:11]2[C:12]3[CH:25]=[CH:24][CH:23]=[CH:22][C:13]=3[S:14][C:15]=2[CH2:16]OS(C)(=O)=O)[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1>CN(C=O)C.O>[N:1]([CH2:16][C:15]1[S:14][C:13]2[CH:22]=[CH:23][CH:24]=[CH:25][C:12]=2[C:11]=1[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[N+:2]=[N-:3]
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 2

HCID 33557Sodium AzideHCID 86668872(3-Phenylbenzo[b]thiophen-2-yl)methyl methanesulfonate

生成物 1

HCID 866688732-Azidomethyl-3-phenylbenzo[b]thiophene収率 50%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

実験手順

Sodium azide (179 mg, 2.76 mmol) was added to a solution of methanesulfonic acid 3-phenylbenzo[b]thiophen-2-ylmethyl ester (828 mg, 1.84 mmol) in DMF (10 mL) and the mixture was stirred at RT for 18 h. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was washed with brine, then dried (Na2SO4) and concentrated in vacuo and the resulting residue was purified by column chromatography (Si—PCC, gradient 0-35% DCM in cyclohexane) affording 2-azidomethyl-3-phenylbenzo[b]thiophene as a clear oil (244 mg, 50%). LCMS: RT 4.46 min [M+H-N2]+ 237.8.

後処理

  1. extractionextracted with EtOAc
  2. washThe organic layer was washed with brine
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated in vacuo
  5. customthe resulting residue was purified by column chromatography (Si—PCC, gradient 0-35% DCM in cyclohexane)

出典と根拠

ORDレコード
ord-ff4f546fd7904f3b988cb0d5783279b6
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08653089B2

反応ノート

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