Ethylene Glycol → HCID 59435991、化合物

HRID 1802489ノート

反応式

HRID 1802489 の反応式
[NH2:1][C:2]1[C:7]([Cl:8])=[CH:6][C:5]([C:9](=[O:11])[CH3:10])=[CH:4][C:3]=1[Cl:12].C1(C)C=CC(S(O)(=O)=O)=CC=1.[NH+]1C=CC=CC=1.[CH2:30](O)[CH2:31][OH:32]>C1C=CC=CC=1>[Cl:12][C:3]1[CH:4]=[C:5]([C:9]2([CH3:10])[O:32][CH2:31][CH2:30][O:11]2)[CH:6]=[C:7]([Cl:8])[C:2]=1[NH2:1]

参加物

5

反応物 3

HCID 174Ethylene GlycolHCID 6048121-(4-Amino-3,5-dichlorophenyl)ethan-1-oneHCID 22033616Pyridinium.p-toluenesulfonate

生成物 1

HCID 59435991HCID 59435991、化合物

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

1-(4-Amino-3,5-dichlorophenyl)ethanone (15 g, 73.5 mmol), pyridinium p-toluene sulfonic acid (5.5 g, 22 mmol), and ethylene glycol (6.2 mL, 110 mmol) were heated together in benzene (250 mL) with a Dean Stark trap at 100° C. overnight. The benzene was distilled off until ˜75 mL remained and the reaction mixture was extracted with EtOAc and saturated NaHCO3. The organic layer was separated, dried with MgSO4, filtered, and concentrated under rotary evaporation to afford a oily residue. The crude mixture was purified on silica gel chromatography (100% Hex to 100% EtOAc) to afford the desired product.

後処理

  1. distillationThe benzene was distilled off until ˜75 mL
  2. extractionthe reaction mixture was extracted with EtOAc and saturated NaHCO3
  3. customThe organic layer was separated
  4. dry with materialdried with MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated under rotary evaporation
  7. customto afford a oily residue
  8. customThe crude mixture was purified on silica gel chromatography (100% Hex to 100% EtOAc)

出典と根拠

ORDレコード
ord-c178203498d5466681c752928b186431
出典データセット
uspto-grants-2013_01
特許番号
US08349865B2

反応ノート

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