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Methanol → Methyl 8-oxooctanoate

HRID 2055072
Notes
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Reaction equation

HRID 2055072 reaction equation
[CH:1]1[CH2:8][CH2:7]CC[CH2:4][CH2:3][CH:2]=1.[C:9](=[O:12])(O)[O-:10].[Na+].Cl[CH2:15]Cl.C(N(CC)CC)C.[CH3:24][OH:25]>>[O:25]=[CH:24][CH2:7][CH2:8][CH2:1][CH2:2][CH2:3][CH2:4][C:9]([O:10][CH3:15])=[O:12]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 887MethanolHCID 6344DichloromethaneHCID 8471TriethylamineHCID 136091-CycloocteneHCID 516892Sodium Bicarbonate

Product 1

HCID 535040Methyl 8-oxooctanoate

Procedure

48 g cyclooctene (1) and 8.4 g sodium bicarbonate were ozonolysed in 48 g methanol and 1 l dichloromethane at −78° C. for 5.5 h. 304 g triethylamine was added slowly dropwise at −60 [lacuna] C and the reaction mixture was allowed to warm to room temperature in the course of 1 h. The reaction mixture was washed with sodium thiosulphate solution (10%, 200 ml), 2 N HCl (150 ml), NaOH (5%, 150 ml) and NaCl solution (saturated, 200 ml) and dried over sodium sulphate and the solvent was distilled off. After distillation, methyl 8-oxooctanoate (2) was obtained.

Workup

  1. washThe reaction mixture was washed with sodium thiosulphate solution (10%, 200 ml), 2 N HCl (150 ml), NaOH (5%, 150 ml) and NaCl solution (saturated, 200 ml)
  2. dry with materialdried over sodium sulphate
  3. distillationthe solvent was distilled off
  4. distillationAfter distillation

Sources & evidence

ORD record
ord-42603ca4faa4454f83dbfb7edc008a5f
Source dataset
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07332468B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes