N-(4-hydroxy-2,3,6-trimethylphenyl)formamide → HCID 73856747, compound

HRID 2211703Notes

Reaction equation

HRID 2211703 reaction equation
[OH:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([NH:9][CH:10]=[O:11])=[C:4]([CH3:12])[C:3]=1[CH3:13].Br[CH2:15][C:16]([CH3:24])=[CH:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>C(OCC)(=O)C.CCCCCC>[CH3:12][C:4]1[C:3]([CH3:13])=[C:2]([O:1][CH2:15][C:16]([CH3:24])=[CH:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:7]=[C:6]([CH3:8])[C:5]=1[NH:9][CH:10]=[O:11]

Participants

4

Reactant 2

HCID 21961295N-(4-hydroxy-2,3,6-trimethylphenyl)formamideHCID 54503384HCID 54503384, compound

Product 1

HCID 73856747HCID 73856747, compoundYield 41%

Reagents, catalysts & solvents 1

HCID 21226206Ethyl acetate hexaneSolvent

Procedure

By using N-(4-hydroxy-2,3,6-trimethylphenyl)formamide and 1-(3-bromo-2-methyl-1-propenyl)benzene, the title compound was synthesized according to Reference Example 17a. Yield: 41%. Melting point: 152-154° C. (Ethyl acetate-hexane).

Sources & evidence

ORD record
ord-2128ee3e2c114df18dd01b6d3c61289c
Source dataset
uspto-grants-2006_09
Patent number
US07101867B2

Reaction notes

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