O-ethylhydroxylamine hydrochloride → 5-(2,6-Dimethyl-4-hydroxyphenyl)-2-[1-(ethoxyimino)propyl]-3-hydroxycyclohex-2-en-1-one

HRID 35783Notes

Reaction equation

HRID 35783 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[C:4]([CH3:9])[C:3]=1[CH:10]1[CH2:15][C:14](=[O:16])[C:13]([C:17](=O)[CH2:18][CH3:19])=[C:12]([OH:21])[CH2:11]1.Cl.[CH2:23]([O:25][NH2:26])[CH3:24]>>[CH3:9][C:4]1[CH:5]=[C:6]([OH:8])[CH:7]=[C:2]([CH3:1])[C:3]=1[CH:10]1[CH2:15][C:14](=[O:16])[C:13]([C:17](=[N:26][O:25][CH2:23][CH3:24])[CH2:18][CH3:19])=[C:12]([OH:21])[CH2:11]1

Participants

3

Reactant 2

HCID 76850O-ethylhydroxylamine hydrochlorideHCID 178458861HCID 178458861, compound

Product 1

HCID 1361995845-(2,6-Dimethyl-4-hydroxyphenyl)-2-[1-(ethoxyimino)propyl]-3-hydroxycyclohex-2-en-1-one

Procedure

5-(2,6-Dimethyl-4-hydroxyphenyl)-2-[1-(ethoxyimino)propyl]-3-hydroxycyclohex-2-en-1-one (31) was prepared from 5-(2,6-dimethyl-4-hydroxyphenyl)-3-hydroxy-2-propionylcyclohex-2-en-1-one and ethoxyamine hydrochloride following essentially the same procedure as that described in Example 1, part (iv). The product was characterized by proton nuclear magnetic resonance spectroscopy and the spectroscopic data is reported in Table 5, Example 37.

Sources & evidence

ORD record
ord-d6a2513d2daa45ca9c05c03ed0d3747b
Source dataset
uspto-grants-1988_08
Patent number
US04767879

Reaction notes

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