3-Chloro-2-methyl-1-propene → N-{2-[(2-Methylprop-2-en-1-yl)oxy]phenyl}acetamide

HRID 584623

Reaction equation

Cl[CH2:2][C:3]([CH3:5])=[CH2:4].[C:6]([NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[OH:16])(=[O:8])[CH3:7]>>[CH3:5][C:3](=[CH2:4])[CH2:2][O:16][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[NH:9][C:6](=[O:8])[CH3:7]

Participants

Reactant 2

HCID 112413-Chloro-2-methyl-1-propene

HCID 119722-Acetamidophenol

Product 1

HCID 13617329N-{2-[(2-Methylprop-2-en-1-yl)oxy]phenyl}acetamideYield 85.5%

Procedure

The compound (1.74 g, 85%) was prepared from 3-chloro-2-methylpropene (1.09 g, 11.9 mmol) and 2-acetamidophenol (1.50 g, 9.92 mmol) analogously to that described in Example 8(i).

Sources & evidence

ORD record: ord-4fc711b018ff4f54a483dcfd6b760f18
Source dataset: uspto-grants-2005_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06927222B2

Linked notes

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