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Hydroquinone → Formaldehyde

HRID 18660
Notes
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Reaction equation

HRID 18660 reaction equation
[C:1]1([OH:7])C=CC=CC=1.[C:8]1([CH:15]=[CH:14][CH:13]=[C:11](O)[CH:10]=1)[OH:9].C1(C=CC(O)=CC=1)O.OC1C=CC(CC2C=CC(O)=CC=2)=CC=1.OC1C=CC(C(C2C=CC(O)=CC=2)(C)C)=CC=1.BrC1C=C(C(C2C=C(Br)C(O)=C(Br)C=2)(C)C)C=C(Br)C=1O.C1C(O)=CC=C(S(C2C=CC(O)=CC=2)(=O)=O)C=1>>[CH2:1]=[O:7].[C:8]1([OH:9])[CH:15]=[CH:14][CH:13]=[CH:11][CH:10]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

9

Reactant 7

HCID 785HydroquinoneHCID 996PhenolHCID 5054ResorcinolHCID 6618Tetrabromobisphenol AHCID 6623Bisphenol AHCID 6626Bisphenol SHCID 12111Bis(4-hydroxyphenyl)methane

Product 2

HCID 712FormaldehydeHCID 996Phenol

Procedure

The epoxide compounds may also derive from monocyclic phenols, for example from phenol, resorcinol or hydroquinone; or they are based on polycyclic phenols, for example bis(4-hydroxyphenyl)methane, 2,2-bis(4-hydroxyphenyl)propane, 2,2-bis(3,5-dibromo-4-hydroxyphenyl)propane, 4,4′-dihydroxydiphenyl sulphone, or condensation products, obtained under acidic conditions, of phenols with formaldehyde, such as phenol novolacs.

Sources & evidence

ORD record
ord-4bf6bc2e75e94f57ae912c00f4ae4b10
Source dataset
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07741390B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes