4-Hydroxybenzyl Alcohol → {7-[4-(3,4-Dichloro-benzyloxy)-benzylsulfanyl]-indan-4-yloxy}-acetic Acid

HRID 1063726Notes

Reaction equation

HRID 1063726 reaction equation
C[O:2][C:3](=[O:16])[CH2:4][O:5][C:6]1[CH:14]=[CH:13][C:12]([SH:15])=[C:11]2[C:7]=1[CH2:8][CH2:9][CH2:10]2.[Cl:17][C:18]1[CH:23]=[CH:22][C:21]([CH2:24][O:25][C:26]2[CH:31]=[CH:30][C:29]([CH2:32]Cl)=[CH:28][CH:27]=2)=[CH:20][C:19]=1[Cl:34].BrCC1C=CC(Cl)=C(Cl)C=1.OCC1C=CC(O)=CC=1.ClCC1(C(F)(F)F)C=CC(OCC2C=CC=CC=2)=CC1>>[Cl:34][C:19]1[CH:20]=[C:21]([CH:22]=[CH:23][C:18]=1[Cl:17])[CH2:24][O:25][C:26]1[CH:31]=[CH:30][C:29]([CH2:32][S:15][C:12]2[CH:13]=[CH:14][C:6]([O:5][CH2:4][C:3]([OH:2])=[O:16])=[C:7]3[C:11]=2[CH2:10][CH2:9][CH2:8]3)=[CH:28][CH:27]=1

Participants

6

Reactant 5

HCID 1254-Hydroxybenzyl AlcoholHCID 6397264-(Bromomethyl)-1,2-dichlorobenzeneHCID 20770872(7-Mercapto-indan-4-yloxy)-acetic Acid Methyl EsterHCID 22280207HCID 22280207, compoundHCID 694705984-Chloromethyl-(4-trifluoromethyl-benzyloxy-benzene)

Product 1

HCID 22280059{7-[4-(3,4-Dichloro-benzyloxy)-benzylsulfanyl]-indan-4-yloxy}-acetic Acid

Procedure

The title compound was prepared in the manner analogous to Example 1F using 12C and 1,2-Dichloro-4-(4-chloromethyl-phenoxymethyl)-benzene prepared from 1-bromomethyl-3,4-dichloro-benzene and 4-hydroxymethyl-phenol in the manner analagous to Examples 14A and 14B. MS m/z 503 (M+1).

Sources & evidence

ORD record
ord-a7ba193a52a04c7ca356d9bf8ed958ec
Source dataset
uspto-grants-2005_11
Patent number
US06964983B2

Reaction notes

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