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Hydrochloric Acid → 3-Acetyl-hexanoic acid

HRID 898692
Notes
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Reaction equation

HRID 898692 reaction equation
C(OC(=O)[C:5]([C:15](=[O:17])[CH3:16])([CH2:12][CH2:13][CH3:14])[CH2:6][C:7]([O:9]CC)=[O:8])C.Cl>[Cl-].[Na+].O>[C:15]([CH:5]([CH2:12][CH2:13][CH3:14])[CH2:6][C:7]([OH:9])=[O:8])(=[O:17])[CH3:16]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 596930242-Acetyl-2-propyl-succinic acid diethyl ester

Product 1

HCID 219192833-Acetyl-hexanoic acid

Reagents, catalysts & solvents 1

HCID 57417360Sodium chloride; waterSolvent

Conditions

Temperature
105 °C

Procedure

To 35 g of 2-acetyl-2-propyl-succinic acid diethyl ester, is added concentrated HCl (200 ml). The mixture is refluxed (oil bath 105° C.) overnight and to it is added brine (100 ml). The mixture is extracted with EtOAc (4×150 ml) and the combined extracts are extracted with 2N aqueous NaOH solution (4×100 ml). The NaOH solution is then cooled to 0° C. and acidified with concentrated HCl. The mixture is extracted with EtOAc (4×200 ml) and the combined extracts are washed with brine (200 ml), dried (Na2SO4) and evaporated in vacuo, which provides the title product as a yellow oil.

Workup

  1. extractionThe mixture is extracted with EtOAc (4×150 ml)
  2. extractionthe combined extracts are extracted with 2N aqueous NaOH solution (4×100 ml)
  3. temperatureThe NaOH solution is then cooled to 0° C.
  4. extractionThe mixture is extracted with EtOAc (4×200 ml)
  5. washthe combined extracts are washed with brine (200 ml)
  6. dry with materialdried (Na2SO4)
  7. customevaporated in vacuo, which

Sources & evidence

ORD record
ord-193391ab9a2546ea8555bbc3878dac60
Source dataset
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07351826B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes