Ethyl 2-bromopropionate → HCID 20142067, compound

HRID 649111Notes

Reaction equation

HRID 649111 reaction equation
[Cl:1][C:2]1[C:11]([O:12][C:13]2[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=2)=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Cl:20])[CH:8]=2)[N:3]=1.Br[CH:22]([CH3:28])[C:23]([O:25][CH2:26][CH3:27])=[O:24]>>[Cl:1][C:2]1[C:11]([O:12][C:13]2[CH:14]=[CH:15][C:16]([O:19][CH:22]([CH3:28])[C:23]([O:25][CH2:26][CH3:27])=[O:24])=[CH:17][CH:18]=2)=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Cl:20])[CH:8]=2)[N:3]=1

Participants

3

Reactant 2

HCID 79040Ethyl 2-bromopropionateHCID 20142093HCID 20142093, compound

Product 1

HCID 20142067HCID 20142067, compound

Procedure

Ethyl 2-{4-[(2,6-dichloroquinolin-3-yl)oxy]phenoxy}propionate was prepared by reacting 4-[(2,6-dichloroquinolin-3-yl)oxy]phenol and ethyl 2-bromopropionate following essentially the same procedure as that described in Example 1 part (c). The product was obtained as a solid, mp 56° C.

Workup

  1. customThe product was obtained as a solid, mp 56° C.

Sources & evidence

ORD record
ord-6a07d10883d0438da50f6e25b85ce3c0
Source dataset
uspto-grants-1988_04
Patent number
US04738710

Reaction notes

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