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Resorcinol → 2-Methylresorcinol

HRID 2083687
Notes
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Reaction equation

HRID 2083687 reaction equation
C1(C=CC=C(O)C=1)O.C1(C=CC=C(O)C1)O.[CH3:17][CH:18]1[C:23](=[O:24])[CH2:22][CH2:21][CH2:20][C:19]1=[O:25].BrBr.BrC1C=C(Br)C(O)=C(C)C=1O>>[CH3:17][C:18]1[C:19]([OH:25])=[CH:20][CH:21]=[CH:22][C:23]=1[OH:24]
ParticipantsProcedureSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 5054ResorcinolHCID 24408BromineHCID 709452-Methyl-1,3-cyclohexanedioneHCID 116141Resorcinol, 4,6-dibromo-2-methyl-HCID 19922823Cyclohexa-3,5-diene-1,3-diol

Product 1

HCID 118432-Methylresorcinol

Procedure

The synthetic routes to an alkylresorcinol that is partially alkylated at a position other than the 4th position on the aromatic ring are multistep and give low overall yields. For example, a 50% yield of a 2-methylresorcinol is obtained by hydrogenation of resorcinol and methylation of the resulting dihydroresorcinol to 2-methylcyclohexane-1,3-dione which on treatment with bromine is converted into 4,6-dibromo-2-methylresorcinol and finally hydrogenolysis of the dibromo derivative to produce the 2-methylresorcinol. Another example is that 5-methylresorcinol can be prepared by a five-step synthesis starting with p-toluidine or a four-step synthesis starting from ethyl crotonate. The five-step synthesis involves acetylation, two-step nitration, reductive hydrogenation, and hydrolysis.

Sources & evidence

ORD record
ord-f4e2d9dc1d0a47828b9533974bdd263c
Source dataset
uspto-grants-1978_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04086281

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes