HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Acetyl chloride → 4-Carbomethoxy-2-methylbutanoic acid

HRID 614869
Notes
Print preview

Reaction equation

HRID 614869 reaction equation
CC(CCC(O)=O)C(O)=O.C(Cl)(=O)C.C1(NC2CCCCC2)CCCCC1.[CH3:28][O:29][C:30]([CH2:32][CH2:33][CH:34]([CH3:38])[C:35]([OH:37])=[O:36])=[O:31]>C(OCC)(=O)C>[CH3:28][O:29][C:30]([CH2:32][CH2:33][CH:34]([CH3:38])[C:35]([OH:37])=[O:36])=[O:31]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6367Acetyl chlorideHCID 120462-Methylglutaric AcidHCID 705834004-Methoxycarbonyl-2-methyl butanoic acid dicyclohexylamine salt

Product 1

HCID 131928974-Carbomethoxy-2-methylbutanoic acid

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

2-Methylglutaric acid (14.6 g.) and acetyl chloride (26 ml.) are heated in the steam bath for one hour. The mixture is concentrated to dryness in vacuo and the residue is evaporated twice from toluene. The residue is dissolved in methanol (4.7 ml.) and heated on the steam bath for one hour and concentrated to dryness. The residue is dissolved in a mixture of ether (17 ml.), dicyclohexylamine (16.7 ml.) and hexane (83 ml.). The crystalline salt is filtered off and the filtrate is concentrated to one third volume and chilled. The crystals are filtered and dried to yield 11.3 g. of 4-methoxycarbonyl-2-methyl butanoic acid dicyclohexylamine salt, m.p. 97°-99°. The salt is converted to the free acid by distribution between ethyl acetate and aqueous acid.

Workup

  1. concentrationThe mixture is concentrated to dryness in vacuo
  2. customthe residue is evaporated twice from toluene
  3. dissolutionThe residue is dissolved in methanol (4.7 ml.)
  4. temperatureheated on the steam bath for one hour
  5. concentrationconcentrated to dryness
  6. dissolutionThe residue is dissolved in a mixture of ether (17 ml.), dicyclohexylamine (16.7 ml.) and hexane (83 ml.)
  7. filtrationThe crystalline salt is filtered off
  8. concentrationthe filtrate is concentrated to one third volume
  9. temperaturechilled
  10. filtrationThe crystals are filtered
  11. customdried
  12. customto yield 11.3 g

Sources & evidence

ORD record
ord-ab940557bcf1458186603e60133c664c
Source dataset
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04146639

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes