2',4'-Dihydroxy-3'-propylacetophenone → HCID 13912820, compound

HRID 652521Notes

Reaction equation

HRID 652521 reaction equation
[OH:1][C:2]1[C:7]([CH2:8][CH2:9][CH3:10])=[C:6]([OH:11])[CH:5]=[CH:4][C:3]=1[C:12](=[O:14])[CH3:13].[CH2:15]([O:17][C:18](=[O:30])[C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([CH2:25]Br)[C:20]=1[O:27][CH2:28][CH3:29])[CH3:16]>>[CH2:15]([O:17][C:18](=[O:30])[C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([CH2:25][O:11][C:6]2[CH:5]=[CH:4][C:3]([C:12](=[O:14])[CH3:13])=[C:2]([OH:1])[C:7]=2[CH2:8][CH2:9][CH3:10])[C:20]=1[O:27][CH2:28][CH3:29])[CH3:16]

Participants

3

Reactant 2

HCID 27751982',4'-Dihydroxy-3'-propylacetophenoneHCID 54409791HCID 54409791, compound

Product 1

HCID 13912820HCID 13912820, compound

Procedure

1-(2,4-dihydroxy-3-propylphenyl)ethanone was allowed to react with 3-(bromomethyl)-2-ethoxybenzoic acid ethyl ester according to the procedure of Example 69 and the product was purified by HPLC to give 3--[(4-acetyl-3-hydroxy-2-propylphenoxy)methyl]-2-ethoxybenzoic acid ethyl ester, the title compound, m.p. 59°-62° in 90% yield.

Workup

  1. customthe product was purified by HPLC

Sources & evidence

ORD record
ord-8f43aa922c654aeea78f39fd50349fe9
Source dataset
uspto-grants-1987_06
Patent number
US04672066

Reaction notes

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