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Chloroacetone → HCID 66806507、化合物

HRID 589656
ノート
印刷プレビュー

反応式

HRID 589656 の反応式
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([SH:10])=[CH:6][CH:5]=1)([CH3:3])[CH3:2].Cl[CH2:12][C:13](=O)[CH3:14].C([O-])([O-])=O.[K+].[K+]>CC(C)=O>[CH:1]([C:4]1[CH:5]=[CH:6][C:7]2[S:10][CH:12]=[C:13]([CH3:14])[C:8]=2[CH:9]=1)([CH3:3])[CH3:2]
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 3

HCID 6571Chloroacetone2 回HCID 11430Potassium Carbonate2 回HCID 5212514-Isopropylbenzenethiol

生成物 1

HCID 66806507HCID 66806507、化合物収率 67.3%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

A mixture of 4-isopropyl-thiophenol (5.0 g, 32.8 mmol), chloroacetone (7.0 mL, 88 mmol) and K2CO3 (6.4 g, 46.3 mmol) in acetone (100 mL) was refluxed over night. More K2CO3 (2 g, 14.5 mmol) and chloroacetone (3.5 mL, 43 mmol) were added and the reaction mixture was heated for another 5 h. The reaction mixture was filtered and the solvent was evaporated. The crude product was mixed with polyphosphoric acid (15 g) and chlorobenzene (100 mL) and the reaction mixture was heated at reflux for 5 h. (Plé et al., (1988) J. Heterocyclic Chem. 25, 1271-1272). The reaction mixture was diluted with CH2Cl2 and washed with water. The combined organic phases were dried and the solvent was evaporated. The crude product was purified on silica using heptane as eluent, giving 4.2 g of the title compound as a colourless oil (67% over two steps). 1H NMR (400 MHz, CDCl3) δ ppm 1.37 (d, 6 H) 2.47 (d, 3 H) 3.02-3.16 (m, 1 H) 7.08 (s, 1 H) 7.27-7.30 (m, 1 H) 7.58 (d, 1 H) 7.80 (d, 1 H).

後処理

  1. temperaturewas refluxed over night
  2. temperaturethe reaction mixture was heated for another 5 h
  3. filtrationThe reaction mixture was filtered
  4. customthe solvent was evaporated
  5. additionThe crude product was mixed with polyphosphoric acid (15 g) and chlorobenzene (100 mL)
  6. temperaturethe reaction mixture was heated
  7. temperatureat reflux for 5 h. (Plé et al., (1988) J. Heterocyclic Chem. 25, 1271-1272)
  8. additionThe reaction mixture was diluted with CH2Cl2
  9. washwashed with water
  10. customThe combined organic phases were dried
  11. customthe solvent was evaporated
  12. customThe crude product was purified on silica

出典と根拠

ORDレコード
ord-11d688a4aee443e88325fce088e7af07
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09233946B2

反応ノート

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