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

Phenol → Bisphenol S

HRID 971970
Notes
Print preview

Reaction equation

HRID 971970 reaction equation
[CH:1]1[C:6]([OH:7])=[CH:5][CH:4]=[C:3]([S:8]([C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=2)(=[O:10])=[O:9])[CH:2]=1.[C:18]1([OH:24])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.S(=O)(=O)(O)O>>[CH:15]1[C:14]([OH:17])=[CH:13][CH:12]=[C:11]([S:8]([C:3]2[CH:4]=[CH:5][C:6]([OH:7])=[CH:1][CH:2]=2)(=[O:10])=[O:9])[CH:16]=1.[CH:22]1[CH:23]=[C:18]([OH:24])[C:19]([S:8]([C:3]2[CH:4]=[CH:5][C:6]([OH:7])=[CH:1][CH:2]=2)(=[O:10])=[O:9])=[CH:20][CH:21]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 996PhenolHCID 1118Sulfuric AcidHCID 6626Bisphenol S

Product 2

HCID 6626Bisphenol SHCID 793812,4'-Dihydroxydiphenyl sulfone

Procedure

It is known to prepare 4,4'-dihydroxydiphenylsulfone from phenol and sulfuric acid. This process yields 4,4'-dihydroxydiphenylsulfone along with large quantities of 2,4'-dihydroxydiphenylsulfone as an isomer by-product. However, extreme difficulty is encountered in separating the 4,4'-dihydroxydiphenylsulfone directly from the resulting reaction mixture.

Sources & evidence

ORD record
ord-e5c6c576762d4a929fc4557e086db4c5
Source dataset
uspto-grants-1979_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04162270

Reaction notes

Loading…

On this pageParticipantsProcedureSources & evidenceReaction notes