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Water → 2-Cyclopentoxy-5-tetrazol-1-ylbenzaldehyde

HRID 376267
ノート
印刷プレビュー

反応式

HRID 376267 の反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:7]([N:10]2[CH:14]=[N:13][N:12]=[N:11]2)=[CH:6][C:3]=1[CH:4]=[O:5].C(=O)([O-])[O-].[K+].[K+].[CH:21]1(Br)[CH2:25][CH2:24][CH2:23][CH2:22]1.O>CN(C)C=O>[CH:21]1([O:1][C:2]2[CH:9]=[CH:8][C:7]([N:10]3[CH:14]=[N:13][N:12]=[N:11]3)=[CH:6][C:3]=2[CH:4]=[O:5])[CH2:25][CH2:24][CH2:23][CH2:22]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 8728BromocyclopentaneHCID 11430Potassium CarbonateHCID 108453442-Hydroxy-5-tetrazol-1-yl-benzaldehyde

生成物 1

HCID 193617862-Cyclopentoxy-5-tetrazol-1-ylbenzaldehyde

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A mixture of 2-hydroxy-5tetrazol-1-yl-benzaldehyde (500 mg) and potassium carbonate (431 mg) in dimethylformamide (5 ml) at 20° was treated with cyclopentyl bromide (0.33 ml). After 24 h water (20 ml) was added and the mixture extracted with ethyl acetate (2×25 ml). The organics were washed with water (25 ml) and brine (25 ml) and dried (Na2SO4). Evaporation gave a yellow solid which was purified by FCC (ethyl acetate/cyclohexane (2:1)) to give the title compound, as a yellow solid (334 mg).

後処理

  1. extractionthe mixture extracted with ethyl acetate (2×25 ml)
  2. washThe organics were washed with water (25 ml) and brine (25 ml)
  3. dry with materialdried (Na2SO4)
  4. customEvaporation
  5. customgave a yellow solid which
  6. customwas purified by FCC (ethyl acetate/cyclohexane (2:1))

出典と根拠

ORDレコード
ord-f3cadf8ca23940e79733b9ddbce6cae0
出典データセット
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06020346

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート