HCID 20827007, compound → HCID 22280028, compound

HRID 1063685Notes

Reaction equation

HRID 1063685 reaction equation
C(C1C=CC(COC2C=CC(CO)=CC=2)=CC=1)(C)(C)C.C[O:22][C:23](=[O:53])[CH2:24][O:25][C:26]1[CH:31]=[CH:30][C:29]([S:32][CH2:33][C:34]2[CH:39]=[CH:38][C:37]([O:40][CH2:41][C:42]3[CH:47]=[CH:46][C:45]([C:48]([CH3:51])([CH3:50])[CH3:49])=[CH:44][CH:43]=3)=[CH:36][CH:35]=2)=[CH:28][C:27]=1[CH3:52]>>[C:48]([C:45]1[CH:46]=[CH:47][C:42]([CH2:41][O:40][C:37]2[CH:38]=[CH:39][C:34]([CH2:33][S:32][C:29]3[CH:30]=[CH:31][C:26]([O:25][CH2:24][C:23]([OH:53])=[O:22])=[C:27]([CH3:52])[CH:28]=3)=[CH:35][CH:36]=2)=[CH:43][CH:44]=1)([CH3:51])([CH3:49])[CH3:50]

Participants

3

Reactant 2

HCID 20827007HCID 20827007, compound2×HCID 22280136HCID 22280136, compound

Product 1

HCID 22280028HCID 22280028, compound

Procedure

The title compound was prepared in the manner analogous to Example 3B using 34A. MS m/z 253 (M-Cl). Step 3. Preparation of {4-[4-(4-tert-Butyl-benzyloxy)-benzylsulfanyl]-2-methyl-phenoxy}-acetic acid methyl ester (Compound 34C)

Sources & evidence

ORD record
ord-f249e830a30a4c96a327315be1d3b86f
Source dataset
uspto-grants-2005_11
Patent number
US06964983B2

Reaction notes

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