Methyl 3-chloro-4-(4-bromobutyloxy)-phenylacetate → Methyl 3-chloro-4-(3-(3-phenyl-7-propylbenzofuran-6-yloxy)butyloxy)-phenylacetate

HRID 342787Notes

Reaction equation

HRID 342787 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:14][C:15]([O:17][CH3:18])=[O:16])[CH:5]=[CH:6][C:7]=1[O:8][CH2:9][CH2:10][CH2:11][CH2:12]Br.[C:19]1([C:25]2[C:29]3[CH:30]=[CH:31][C:32]([OH:37])=[C:33]([CH2:34][CH2:35][CH3:36])[C:28]=3[O:27][CH:26]=2)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[Cl:1][C:2]1[CH:3]=[C:4]([CH2:14][C:15]([O:17][CH3:18])=[O:16])[CH:5]=[CH:6][C:7]=1[O:8][CH2:9][CH2:10][CH:11]([O:37][C:32]1[CH:31]=[CH:30][C:29]2[C:25]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)=[CH:26][O:27][C:28]=2[C:33]=1[CH2:34][CH2:35][CH3:36])[CH3:12]

Participants

3

Reactant 2

HCID 15290476Methyl 3-chloro-4-(4-bromobutyloxy)-phenylacetateHCID 154629143-Phenyl-7-propyl-1-benzofuran-6-ol

Product 1

HCID 53704249Methyl 3-chloro-4-(3-(3-phenyl-7-propylbenzofuran-6-yloxy)butyloxy)-phenylacetate

Procedure

Using the method of Example 19, step E, using methyl 3-chloro-4-(4-bromobutyloxy)-phenylacetate (Example 8, Step 2) and 3-phenyl-6-hydroxy-7-propylbenzofuran (Example 5, Step B) as the starting material, the title compound was obtained.

Sources & evidence

ORD record
ord-9fd452f34ce54d6c9516fa849b5d17cc
Source dataset
uspto-grants-1999_01
Patent number
US05859051

Reaction notes

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