Methyl 3,5-dihydroxyphenylacetate → HCID 131729542, compound

HRID 1686441Notes

Reaction equation

HRID 1686441 reaction equation
[CH2:1]([S:3]([C:6]1[CH:11]=[CH:10][C:9](F)=[C:8]([Cl:13])[CH:7]=1)(=[O:5])=[O:4])[CH3:2].[CH3:14][O:15][C:16](=[O:26])[CH2:17][C:18]1[CH:23]=[C:22]([OH:24])[CH:21]=[C:20]([OH:25])[CH:19]=1>>[CH3:14][O:15][C:16](=[O:26])[CH2:17][C:18]1[CH:23]=[C:22]([OH:24])[CH:21]=[C:20]([O:25][C:9]2[CH:10]=[CH:11][C:6]([S:3]([CH2:1][CH3:2])(=[O:5])=[O:4])=[CH:7][C:8]=2[Cl:13])[CH:19]=1

Participants

3

Reactant 2

HCID 579787Methyl 3,5-dihydroxyphenylacetateHCID 579047252-Chloro-4-(ethylsulfonyl)-1-fluorobenzene

Product 1

HCID 131729542HCID 131729542, compound

Procedure

The subtitle compound was prepared as described in example 2 step (iii) but instead using the product from example 3 step (i) and methyl(3,5-dihydroxyphenyl)acetate.

Sources & evidence

ORD record
ord-ce6347a119f3404da26a8c8695810372
Source dataset
uspto-grants-2012_04
Patent number
US08148572B2

Reaction notes

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