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1,1,2,2-Tetrachloroethane → 4-(4-Tert-butylphenyl)-4-oxobutanoic acid

HRID 240298
Notes
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Reaction equation

HRID 240298 reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[C:5]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)([CH3:8])([CH3:7])[CH3:6].[C:15]1(=[O:21])[O:20][C:18](=[O:19])[CH2:17][CH2:16]1.ClC(Cl)C(Cl)Cl>Cl>[C:5]([C:9]1[CH:14]=[CH:13][C:12]([C:15](=[O:21])[CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[CH:11][CH:10]=1)([CH3:8])([CH3:7])[CH3:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 65911,1,2,2-TetrachloroethaneHCID 7366Tert-ButylbenzeneHCID 7922Succinic anhydrideHCID 6451240Aluminum(III) Chloride2×

Product 1

HCID 20640374-(4-Tert-butylphenyl)-4-oxobutanoic acid

Reagents, catalysts & solvents 1

HCID 313
Hydrochloric Acid
Solvent

Procedure

Aluminum chloride powder (80.0 g, 600 mmol) was added in portions to a stirred mixture of tert-butylbenzene (40.0 g, 300 mmol) and succinic anhydride (26.7 g, 267 mmol) and 1,1,2,2-tetrachloroethane (100 mL). After all the aluminum chloride had been added, the mixture was poured into a mixture of ice (500 mL) and concentrated hydrochloric acid (100 mL). The organic layer was separated, washed with water (500 mL) and the solvent distilled off. Solid residue was dissolved in hot 15% aqueous solution of sodium carbonate (1000 mL), filtered, cooled and the acid was precipitated with hydrochloric acid (acidified to pH=1). The crude acid was filtered, dried on air and recrystalised from benzene (500 mL) to give 4-(4-tert-butyl-phenyl)-4-oxo-butyric acid as colorless crystals.

Workup

  1. customThe organic layer was separated
  2. washwashed with water (500 mL)
  3. distillationthe solvent distilled off
  4. dissolutionSolid residue was dissolved in hot 15% aqueous solution of sodium carbonate (1000 mL)
  5. filtrationfiltered
  6. temperaturecooled
  7. customthe acid was precipitated with hydrochloric acid (acidified to pH=1)
  8. filtrationThe crude acid was filtered
  9. customdried on air
  10. customrecrystalised from benzene (500 mL)

Sources & evidence

ORD record
ord-0447b6ba55d24bab9ef590255a74361a
Source dataset
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08648041B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes