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Ethanol → Diisopropyl ether ethanol

HRID 1582613
ノート
印刷プレビュー

反応式

HRID 1582613 の反応式
FC(F)(F)C1C=CC(CN([C:12]2[CH:17]=[CH:16]C(C#N)=CC=2)N)=CC=1.CO[CH:24]([O:29]C)[CH2:25]N=C=S.[CH2:31]([OH:33])[CH3:32]>>[CH:24]([O:29][CH:17]([CH3:16])[CH3:12])([CH3:31])[CH3:25].[CH2:31]([OH:33])[CH3:32]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 702EthanolHCID 144710Isothiocyanatoacetaldehyde dimethyl acetalHCID 12985733N1-(4-trifluoromethylphenylmethyl)-N1-(4-cyanophenyl)hydrazine

生成物 1

HCID 23358034Diisopropyl ether ethanol

実験手順

To a suspension of N1-(4-trifluoromethylphenylmethyl)-N1-(4-cyanophenyl)hydrazine (7.5 g, 0.025 mol) in ethanol (100 ml) was added dropwise 2,2-dimethoxyethylisothiocyanate (4 g, 0.027 mol) and the reaction mixture was heated to reflux for 2 h. After cooling the solvent was evaporated under vacuum, the resulting residue was poured into 2N H2SO4 (20 ml) and the suspension was heated to reflux for 0.3 h. After extraction with ethyl acetate, the organic layer was washed with water, dried over sodium sulfate and concentrated under vacuum. Flash chromatography on silica gel (toluene/dioxane: 8/2) and trituration from diisopropyl ether/ethanol afforded a yellow solid (2.7 g, 28%), mp 200° C.

後処理

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux for 2 h
  3. temperatureAfter cooling the solvent
  4. customwas evaporated under vacuum
  5. additionthe resulting residue was poured into 2N H2SO4 (20 ml)
  6. temperaturethe suspension was heated
  7. temperatureto reflux for 0.3 h
  8. extractionAfter extraction with ethyl acetate
  9. washthe organic layer was washed with water
  10. dry with materialdried over sodium sulfate
  11. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-d32030b38bc64f40ab0975509e3cee5b
出典データセット
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06737433B1

反応ノート

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