HCID 20827047, compound → HCID 10288804, compound

HRID 1063671Notes

Reaction equation

HRID 1063671 reaction equation
FC(F)(F)OC1C=C(C2C=CC=C(CO)C=2)C=CC=1.C[O:21][C:22](=[O:53])[CH2:23][O:24][C:25]1[CH:30]=[C:29]([O:31][CH3:32])[C:28]([S:33][CH2:34][C:35]2[CH:36]=[C:37]([C:41]3[CH:46]=[CH:45][CH:44]=[C:43]([O:47][C:48]([F:51])([F:50])[F:49])[CH:42]=3)[CH:38]=[CH:39][CH:40]=2)=[CH:27][C:26]=1[CH3:52]>>[CH3:32][O:31][C:29]1[C:28]([S:33][CH2:34][C:35]2[CH:36]=[C:37]([C:41]3[CH:46]=[CH:45][CH:44]=[C:43]([O:47][C:48]([F:51])([F:50])[F:49])[CH:42]=3)[CH:38]=[CH:39][CH:40]=2)=[CH:27][C:26]([CH3:52])=[C:25]([CH:30]=1)[O:24][CH2:23][C:22]([OH:53])=[O:21]

Participants

3

Reactant 2

HCID 20827047HCID 20827047, compound2×HCID 22280167HCID 22280167, compound

Product 1

HCID 10288804HCID 10288804, compound

Procedure

The title compound was prepared in the manner analogous to Example 3B using 16A. MS m/z 251 (M−1). Step 2. Preparation of [5-Methoxy-2-methyl-4-(3′-trifluoromethoxy-biphenyl-3-ylmethylsulfanyl)-phenoxy]-acetic acid methyl ester (Compound 16C)

Sources & evidence

ORD record
ord-f4ae51772971494bbd69eeffd8f81ad3
Source dataset
uspto-grants-2005_11
Patent number
US06964983B2

Reaction notes

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