Sodium Hydroxide → HCID 58822712, compound

HRID 459248Notes

Reaction equation

HRID 459248 reaction equation
C([O:3][C:4](=[O:20])[C@@H:5]([O:18][CH3:19])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH2:14][CH2:15][CH2:16]Br)=[CH:9][CH:8]=1)C.[Cl:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[C:28]([C:30]1[CH:35]=[CH:34][C:33]([OH:36])=[CH:32][CH:31]=1)=[O:29].[OH-].[Na+]>>[Cl:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[C:28]([C:30]1[CH:35]=[CH:34][C:33]([O:36][CH2:16][CH2:15][CH2:14][O:13][C:10]2[CH:9]=[CH:8][C:7]([CH2:6][C@H:5]([O:18][CH3:19])[C:4]([OH:3])=[O:20])=[CH:12][CH:11]=2)=[CH:32][CH:31]=1)=[O:29]

Participants

4

Reactant 3

HCID 14798Sodium HydroxideHCID 6432544HCID 6432544, compoundHCID 58822859(2S)-3-[4-(3-Bromopropoxy)-phenyl]-2-methoxy-propionic acid ethyl ester

Product 1

HCID 58822712HCID 58822712, compound

Procedure

(2S)-3-[4-(3-Bromo-propoxy)-phenyl]-2-methoxy-propionic acid ethyl ester from Example 173, Step A was treated with (2-Chloro-phenyl)-(4-hydroxy-phenyl)-methanone from Step B under the Standard Procedure J. The compound thus obtained was allowed to react under Standard hydrolysis procedure C (NaOH) to give the title compound. MS(ES) for C26H25ClO6 [M+NH4]+: 491, [M+H]+: 469.

Workup

  1. customThe compound thus obtained

Sources & evidence

ORD record
ord-3c2b0b91e8154a0ab1ce6d3835fe83f7
Source dataset
uspto-grants-2007_03
Patent number
US07192982B2

Reaction notes

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