HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Imidazole → 4-Trimethylsiloxy-4-vinyl-1-iodo-trans-1-octene

HRID 460934
Notes
Print preview

Reaction equation

HRID 460934 reaction equation
[OH:1][C:2]([CH:11]=[CH2:12])([CH2:7][CH2:8][CH2:9][CH3:10])[CH2:3]/[CH:4]=[CH:5]/[I:6].N1C=CN=C1.Cl[Si:19]([CH3:22])([CH3:21])[CH3:20]>CN(C)C=O>[CH3:20][Si:19]([CH3:22])([CH3:21])[O:1][C:2]([CH:11]=[CH2:12])([CH2:7][CH2:8][CH2:9][CH3:10])[CH2:3]/[CH:4]=[CH:5]/[I:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 795ImidazoleHCID 6397ChlorotrimethylsilaneHCID 128512814-Hydroxy-4-vinyl-1-iodo-trans-1-octene

Product 1

HCID 128512834-Trimethylsiloxy-4-vinyl-1-iodo-trans-1-octene

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

To a stirred solution of 456 mg of 4-hydroxy-4-vinyl-1-iodo-trans-1-octene and 320 mg of imidazole in 1.0 ml of dimethylformamide is added 0.23 ml of chlorotrimethylsilane during 3 minutes. The mixture is stirred at room temperature for 22 hours and partitioned with a mixture of cold hexane and water. The hexane layer is washed repeatedly with water and then brine, dried over magnesium sulfate, and concentrated to give an oil, pmr spectrum (CDCl3): 0.13 (s, trimethylsiloxy group) and 2.32 (d, =CHCH2).

Workup

  1. custompartitioned with a mixture of cold hexane and water
  2. washThe hexane layer is washed repeatedly with water
  3. dry with materialbrine, dried over magnesium sulfate
  4. concentrationconcentrated
  5. customto give an oil, pmr spectrum (CDCl3)

Sources & evidence

ORD record
ord-a8d6c6ef636e4694a8b78a65571918c4
Source dataset
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04061670

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes