Potassium Carbonate → HCID 57863128, compound

HRID 418101Notes

Reaction equation

HRID 418101 reaction equation
[CH2:1]([O:3][C:4](=[O:29])[CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20]Br)[C:10]=1[CH2:22][CH2:23][C:24]([O:26][CH2:27][CH3:28])=[O:25])[CH3:2].[Br:30][C:31]1[CH:32]=[C:33]([OH:42])[CH:34]=[C:35]([S:37]([CH2:40][CH3:41])(=[O:39])=[O:38])[CH:36]=1.C(=O)([O-])[O-].[K+].[K+]>>[CH2:1]([O:3][C:4](=[O:29])[CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][O:42][C:33]2[CH:34]=[C:35]([S:37]([CH2:40][CH3:41])(=[O:39])=[O:38])[CH:36]=[C:31]([Br:30])[CH:32]=2)[C:10]=1[CH2:22][CH2:23][C:24]([O:26][CH2:27][CH3:28])=[O:25])[CH3:2]

Participants

4

Reactant 3

HCID 11430Potassium CarbonateHCID 575864914-[3-(6-Bromo-hexyl)-2-(ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl esterHCID 578630883-Bromo-5-ethanesulfonyl-phenol

Product 1

HCID 57863128HCID 57863128, compoundYield 95%

Procedure

A similar procedure as described in Example 40, step 6 was used, starting from 4-[3-(6-bromo-hexyl)-2-(2-ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl ester (1.13 g, 2.39 mmol), 3-bromo-5-ethanesulfonyl-phenol (576 mg, 2.17 mmol), and potassium carbonate (600 mg, 4.34 mmol) to afford 4-[3-[6-(3-bromo-5-ethanesulfonyl-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl ester (1.35 g, 95%) as a colorless viscous oil: ES(+)-HRMS m/e calcd for C31H43BrO8S (M+Na)+ 677.1754, found 677.1756.

Sources & evidence

ORD record
ord-1f463ab4e13b409084a6741bca9fd496
Source dataset
uspto-grants-2012_01
Patent number
US08093253B2

Reaction notes

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