4-tert-Butylcatechol → HCID 15289112, compound

HRID 1603213Notes

Reaction equation

HRID 1603213 reaction equation
[C:1]1(=[O:7])[NH:5][C:4](=[O:6])[CH:3]=[CH:2]1.[C:8]1([C:14]([O:16][CH2:17][CH3:18])=[O:15])[CH2:13][CH2:12][CH:11]=[CH:10][CH:9]=1.C(C1C=C(O)C(=CC=1)O)(C)(C)C>C1(C)C=CC=CC=1>[CH2:17]([O:16][C:14]([C:8]12[CH2:13][CH2:12][CH:11]([CH:10]=[CH:9]1)[CH:3]1[CH:2]2[C:1](=[O:7])[NH:5][C:4]1=[O:6])=[O:15])[CH3:18]

Participants

5

Reactant 3

HCID 73814-tert-ButylcatecholHCID 10935MaleimideHCID 110948161,3-Cyclohexadiene-1-carboxylic acid, ethyl ester

Product 1

HCID 15289112HCID 15289112, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

13.5 g (0.138 mol) of maleimide and 25.3 g (0.17 mol) of ethyl 1,3-cyclohexadiene-1-carboxylate are heated under reflux with 1.4 g of 4-(tert-butyl)pyrocatechol in 275 ml of toluene overnight. The mixture is concentrated and the residue is recrystallized from isopropanol.

Workup

  1. concentrationThe mixture is concentrated
  2. customthe residue is recrystallized from isopropanol

Sources & evidence

ORD record
ord-1cf43784c2d54a018950786a8b405149
Source dataset
uspto-grants-1999_11
Patent number
US05986105

Reaction notes

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