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Vinyl Acetate → (R)-methyl 9-hydroxy-10-undecenate

HRID 395932
Notes
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Reaction equation

HRID 395932 reaction equation
[OH:1][CH:2]([CH:14]=[CH2:15])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:12][CH3:13])=[O:11].C(OC=C)(=O)C>C(OC(C)C)(C)C>[OH:1][C@@H:2]([CH:14]=[CH2:15])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:12][CH3:13])=[O:11]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 7904Vinyl AcetateHCID 11127632Methyl 9-hydroxy-10-undecenate

Product 1

HCID 11736036(R)-methyl 9-hydroxy-10-undecenateYield 30.4%

Reagents, catalysts & solvents 1

HCID 7914Diisopropyl EtherSolvent

Conditions

Temperature
30 °C

Procedure

To a solution of methyl 9-hydroxy-10-undecenate (500 mg) in diisopropyl ether (12 ml) was added vinyl acetate (323 μl) and Lipase PS (AMANO SEIYAKU Co., Ltd.) (500 mg) and then shaken for 62 hours at 30° C. The reaction mixture was filtrated and the filtrate was poured into ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate anhydride, and then evaporated under reduced pressure. The resulting product was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1) to give (R)-methyl 9-hydroxy-10-undecenate (152 mg, 30.4%).

Workup

  1. filtrationThe reaction mixture was filtrated
  2. additionthe filtrate was poured into ethyl acetate
  3. washThe organic layer was washed with saturated brine
  4. dry with materialdried over magnesium sulfate anhydride
  5. customevaporated under reduced pressure
  6. customThe resulting product was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1)

Sources & evidence

ORD record
ord-b46dbf12afe94e36857135fb52f2566b
Source dataset
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06605741B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes