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

Hydrogen Bromide → 3,3'-Difluoro-4,4'-dihydroxybiphenyl

HRID 2072828
Notes
Print preview

Reaction equation

HRID 2072828 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:10]2[CH:15]=[CH:14][C:13]([O:16]C)=[C:12]([F:18])[CH:11]=2)[CH:5]=[CH:6][C:7]=1[O:8]C.Br>O1CCOCC1>[F:1][C:2]1[CH:3]=[C:4]([C:10]2[CH:15]=[CH:14][C:13]([OH:16])=[C:12]([F:18])[CH:11]=2)[CH:5]=[CH:6][C:7]=1[OH:8]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 260Hydrogen BromideHCID 197520453,3'-Difluoro-4,4'-dimethoxy-1,1'-biphenyl

Product 1

HCID 5209563,3'-Difluoro-4,4'-dihydroxybiphenyl

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

10.0 g of 3,3'-difluoro-4,4'-dimethoxybiphenyl was dissolved in 150 ml of dioxane, and 150 ml of 48% hydrobromic acid was added. The mixture was heated under reflux for 50 hours. After the reaction, the reaction mixture was subjected to evaporation under reduced pressure. The residue was fully washed with water to obtain the desired 3,3'-difluoro-4,4'-dihydroxybiphenyl.

Workup

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 50 hours
  3. customAfter the reaction
  4. customthe reaction mixture was subjected to evaporation under reduced pressure
  5. washThe residue was fully washed with water

Sources & evidence

ORD record
ord-22eec997dd984271a95b2777c6cc5e19
Source dataset
uspto-grants-1990_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04914224

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes