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Methyl Acrylate → 1,5-Dimethyl 2-methylenepentanedioate

HRID 83507
Notes
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Reaction equation

HRID 83507 reaction equation
[C:1]([O:5][CH3:6])(=[O:4])[CH:2]=[CH2:3]>O1CCCC1>[CH3:6][O:5][C:1](=[O:4])[C:2](=[CH2:3])[CH2:3][CH2:2][C:1]([O:5][CH3:6])=[O:4]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 7294Methyl Acrylate

Product 1

HCID 5745371,5-Dimethyl 2-methylenepentanedioate

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

To a solution of 2,8,9-triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo(3,3,3)indecane (4.62 g) in tetrahydrofuran (180 ml) was added dropwise a solution of methyl acrylate (40.5 ml) in tetrahydrofuran (20 ml) at room temperature, and then the mixture was stirred overnight. This reaction solution was concentrated under reduced pressure, and then diisopropyl ether, n-hexane and chloroform were added to the resulting residue, and the mixture was again concentrated under reduced pressure. To the precipitated solid was added diisopropyl ether, the mixture was stirred, and then the insoluble substance was filtered off. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1 to 4/1) to give the titled compound (19.2 g).

Workup

  1. concentrationThis reaction solution was concentrated under reduced pressure
  2. additiondiisopropyl ether, n-hexane and chloroform were added to the resulting residue
  3. concentrationthe mixture was again concentrated under reduced pressure
  4. additionTo the precipitated solid was added diisopropyl ether
  5. stirringthe mixture was stirred
  6. filtrationthe insoluble substance was filtered off
  7. concentrationThe filtrate was concentrated under reduced pressure
  8. customthe resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1 to 4/1)

Sources & evidence

ORD record
ord-61ad8dd423bd402bb78204cfd03c592f
Source dataset
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08846746B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes