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3-Methyl-2-buten-1-OL → 3-Methylbut-2-enyl 2-methylisocrotonate

HRID 65315
Notes
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Reaction equation

HRID 65315 reaction equation
[C:1]([O:7][CH3:8])(=[O:6])/[C:2](=[CH:4]\[CH3:5])/[CH3:3].[CH3:9][C:10]([CH3:14])=[CH:11]CO.C([O-])(=O)CCCCCCCCCCC.C([Sn+2]CCCCCCCC)CCCCCCC.C([O-])(=O)CCCCCCCCCCC>C1(C)C=CC=CC=1>[C:1]([O:7][CH2:8][CH:9]=[C:10]([CH3:14])[CH3:11])(=[O:6])/[C:2](=[CH:4]\[CH3:5])/[CH3:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 111733-Methyl-2-buten-1-OLHCID 5356352Methyl (2Z)-2-methyl-2-butenoateHCID 22292224Dioctyltin laurate

Product 1

HCID 64329433-Methylbut-2-enyl 2-methylisocrotonate

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

A mixture of 19.6 g. of methyl angelate, 22.2 g. of 3-methyl-2-butenyl alcohol, 100 ml. of toluene and 1.6 g. of dioctyltin laurate was placed in a glass flask which was equipped with a Soxhlet extractor filled with molecular sieve 4A on the top and a reflux cooler. The mixture was heated under reflux while returning the refluxed liquid through the molecular sieve 4A to the flask. The mixture obtained from the heating for a total of 26 hours was subjected to single distillation to give 24.24 g. of a distillate boiling at 102°-105° C. (25 mmHg).

Workup

  1. additionA mixture of 19.6 g
  2. customwhich was equipped with a Soxhlet extractor
  3. temperatureThe mixture was heated
  4. temperatureunder reflux
  5. customThe mixture obtained from the heating for a total of 26 hours
  6. distillationwas subjected to single distillation
  7. customto give 24.24 g

Sources & evidence

ORD record
ord-08896e7ec06642c78abc4d95b1516e9c
Source dataset
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04613680

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes