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Isopropanol → Methyl 5-bromo-2-oxopentanoate

HRID 1249531
Notes
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Reaction equation

HRID 1249531 reaction equation
CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O.[Br:14][CH2:15][CH2:16][CH2:17][CH:18]([OH:23])[C:19]([O:21][CH3:22])=[O:20].C(O)(C)C>CC(C)=O.O>[Br:14][CH2:15][CH2:16][CH2:17][C:18](=[O:23])[C:19]([O:21][CH3:22])=[O:20]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 3776IsopropanolHCID 13769948Methyl 5-bromo-2-hydroxypentanoateHCID 131709961Jones' reagent

Product 1

HCID 13769949Methyl 5-bromo-2-oxopentanoateYield 92%

Reagents, catalysts & solvents 2

HCID 180AcetoneSolventHCID 962
Water
Solvent

Procedure

Jones' reagent (CrO3 : 9.58 g, H2SO4 : 8.47 ml, H2O: 36.8 ml) was added to a magnetically stirred solution of Part (3) compound (12.53 g, 59.3 mmole) in acetone (150 ml) at room temperature. The addition was controlled to maintain the temperature below 35° C. After the completion of the addition, the reaction was stirred at room temperature for 45 minutes. Isopropyl alcohol (30 ml) was added dropwise and stirred for 30 minutes. The reaction was then diluted with H2O (500 ml) and the products were extracted with CH2Cl2 (1 l.). The CH2Cl2 layer was washed with brine (100 ml×3) and dried over MgSO4. Filtration and evaporation of solvents gave the title compound (11.4 g, 54.5 mmole, 92%) as a colorless liquid.

Workup

  1. additionThe addition
  2. temperatureto maintain the temperature below 35° C
  3. additionAfter the completion of the addition
  4. stirringstirred for 30 minutes
  5. extractionthe products were extracted with CH2Cl2 (1 l.)
  6. washThe CH2Cl2 layer was washed with brine (100 ml×3)
  7. dry with materialdried over MgSO4
  8. filtrationFiltration and evaporation of solvents

Sources & evidence

ORD record
ord-79f2efaf88654c86982ed7192d7666f1
Source dataset
uspto-grants-1986_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04632931

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes