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Sodium Azide → 4-(Azidomethyl)-2,6-dihydroxymethyl-s-triazine

HRID 495887
ノート
印刷プレビュー

反応式

HRID 495887 の反応式
C1(C)C=CC(S([CH2:10][C:11]2[N:16]=[C:15]([CH2:17][OH:18])[N:14]=[C:13]([CH2:19][OH:20])[N:12]=2)(=O)=O)=CC=1.[N-:22]=[N+:23]=[N-:24].[Na+]>CN(C=O)C>[N:22]([CH2:10][C:11]1[N:12]=[C:13]([CH2:19][OH:20])[N:14]=[C:15]([CH2:17][OH:18])[N:16]=1)=[N+:23]=[N-:24]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 33557Sodium AzideHCID 223236944-(p-Toluenesulfonylmethyl)-2,6-dihydroxymethyl-s-triazine

生成物 1

HCID 223236434-(Azidomethyl)-2,6-dihydroxymethyl-s-triazine

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
50 °C

実験手順

4-(p-Toluenesulfonylmethyl)-2,6-dihydroxymethyl-s-triazine is dissolved in DMF and sodium azide (1.1 eq.) is added. The reaction mixture is heated to 50° C. for 4 hours. The DMF is removed under reduced pressure and the residue is partitioned between CH2Cl2 and water. The CH2Cl2 layer is separated and the water layer is extracted several times with CH2Cl2. The CH2Cl2 layers are combined, dried (MgSO4), and concentrated. The resultant residue is purified by silica gel flash column chromatography to give 4-(azidomethyl)-2,6-dihydroxymethyl-s-triazine.

後処理

  1. customThe DMF is removed under reduced pressure
  2. customthe residue is partitioned between CH2Cl2 and water
  3. customThe CH2Cl2 layer is separated
  4. extractionthe water layer is extracted several times with CH2Cl2
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated
  7. customThe resultant residue is purified by silica gel flash column chromatography

出典と根拠

ORDレコード
ord-29d4037771374b3b8268aa2005f967be
出典データセット
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06942966B1

反応ノート

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