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

Carbon tetrabromide → HCID 22279681, compound

HRID 1869692
Notes
Print preview

Reaction equation

HRID 1869692 reaction equation
[C:1]([Br:5])(Br)(Br)[Br:2].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH:25]1([O:31][CH2:32][CH2:33][CH:34]=O)[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]1>ClCCl>[CH:25]1([O:31][CH2:32][CH2:33][CH:34]=[C:1]([Br:5])[Br:2])[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 22279671HCID 22279671, compound

Product 1

HCID 22279681HCID 22279681, compoundYield 73.4%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent4×

Procedure

Subsequently, to a solution of carbon tetrabromide (36.5 g, 0.11 mol) in dichloromethane (120 ml) was added a solution of triphenylphosphine (57.7 g, 0.22 mol) in dichloromethane (120 ml) with stirring while ice-cooling under a nitrogen atmosphere, and the resulting mixture was stirred for 5 minutes. After stirring, to the reaction mixture was added a solution of the crude 3-cyclohexyloxypropionaldehyde (8.60 g) obtained above in dichloromethane (90 ml) with stirring while ice-cooling under a nitrogen atmosphere, and the resulting mixture was stirred at the same temperature for 25 minutes. After stirring, the reaction mixture was diluted with dichloromethane and washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. After filtration, the solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of hexane and ethyl acetate (100:1-33:1) as the eluent to afford 4-cyclohexyloxy-1,1-dibromobut-1-ene (12.6 g, overall yield in two steps: 55%).

Workup

  1. temperaturecooling under a nitrogen atmosphere
  2. stirringthe resulting mixture was stirred for 5 minutes
  3. stirringAfter stirring, to the reaction mixture
  4. stirringwith stirring while ice-
  5. temperaturecooling under a nitrogen atmosphere
  6. stirringthe resulting mixture was stirred at the same temperature for 25 minutes
  7. stirringAfter stirring
  8. washwashed successively with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution
  9. dry with materialdried over anhydrous sodium sulfate
  10. filtrationAfter filtration
  11. customthe solvent was removed in vacuo
  12. customthe residue was purified by chromatography on a silica gel column

Sources & evidence

ORD record
ord-9b4e73f81161432cae6e245ebe5e568b
Source dataset
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07638551B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes