{4-[(2,4-dichlorobenzyl)oxy]phenyl}methanol → HCID 22280008, compound

HRID 1063681Notes

Reaction equation

HRID 1063681 reaction equation
ClC1C=C(Cl)C=CC=1COC1C=CC(CO)=CC=1.C[O:20][C:21](=[O:49])[CH2:22][O:23][C:24]1[CH:29]=[CH:28][C:27]([S:30][CH2:31][C:32]2[CH:37]=[CH:36][C:35]([O:38][CH2:39][C:40]3[CH:45]=[CH:44][C:43]([Cl:46])=[CH:42][C:41]=3[Cl:47])=[CH:34][CH:33]=2)=[CH:26][C:25]=1[CH3:48]>>[Cl:47][C:41]1[CH:42]=[C:43]([Cl:46])[CH:44]=[CH:45][C:40]=1[CH2:39][O:38][C:35]1[CH:36]=[CH:37][C:32]([CH2:31][S:30][C:27]2[CH:28]=[CH:29][C:24]([O:23][CH2:22][C:21]([OH:49])=[O:20])=[C:25]([CH3:48])[CH:26]=2)=[CH:33][CH:34]=1

Participants

3

Reactant 2

HCID 2763433{4-[(2,4-dichlorobenzyl)oxy]phenyl}methanolHCID 20827020HCID 20827020, compound2×

Product 1

HCID 22280008HCID 22280008, compound

Procedure

The title compound was prepared in the manner analogous to Example 3B using 32A. MS m/z 265 (M-Cl). Step 3. Preparation of {4-[4-(2,4-Dichloro-benzyloxy)-benzylsulfanyl]-2-methyl-phenoxy}-acetic acid methyl ester (Compound 32C)

Sources & evidence

ORD record
ord-662e6467016245d5b619dc5b6646863f
Source dataset
uspto-grants-2005_11
Patent number
US06964983B2

Reaction notes

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