HCID 20827022, compound → HCID 22280061, compound

HRID 1063680Notes

Reaction equation

HRID 1063680 reaction equation
FC1C=C(F)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]([F:46])=[CH:42][C:41]=3[F:47])=[CH:34][CH:33]=2)=[CH:26][C:25]=1[CH3:48]>>[F:47][C:41]1[CH:42]=[C:43]([F: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 20827022HCID 20827022, compound2×HCID 22280034HCID 22280034, compound

Product 1

HCID 22280061HCID 22280061, compound

Procedure

The title compound was prepared in the manner analogous to Example 3B using 31A. MS m/z 233 (M-Cl). Step 3. Preparation of {4-[4-(2,4-Difluoro-benzyloxy)-benzylsulfanyl]-2-methyl-phenoxy}-acetic acid methyl ester (Compound 31C)

Sources & evidence

ORD record
ord-069e7a9d284544f4b1c9cd0d6c9a8f83
Source dataset
uspto-grants-2005_11
Patent number
US06964983B2

Reaction notes

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