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Chloroacetone → HCID 66806507, compound

HRID 589656
Notes
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Reaction equation

HRID 589656 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

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

Product 1

HCID 66806507HCID 66806507, compoundYield 67.3%

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

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).

Workup

  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

Sources & evidence

ORD record
ord-11d688a4aee443e88325fce088e7af07
Source dataset
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09233946B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes