3-Chlorobenzyl alcohol → HCID 68614494, compound

HRID 1823029Notes

Reaction equation

HRID 1823029 reaction equation
[CH3:1][O:2][C:3]([C@@H:5]1[CH2:9][C:8](=[O:10])[N:7]([C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=2)[CH2:6]1)=[O:4].[Cl:18][C:19]1[CH:20]=[C:21]([CH:24]=[CH:25][CH:26]=1)[CH2:22]O>>[CH3:1][O:2][C:3]([C@@H:5]1[CH2:9][C:8](=[O:10])[N:7]([C:11]2[CH:12]=[CH:13][C:14]([O:17][CH2:22][C:21]3[CH:24]=[CH:25][CH:26]=[C:19]([Cl:18])[CH:20]=3)=[CH:15][CH:16]=2)[CH2:6]1)=[O:4]

Participants

3

Reactant 2

HCID 701173-Chlorobenzyl alcoholHCID 785702(R)-1-(4-hydroxyphenyl)-5-oxo-pyrrolidine-3-carboxylic acid methyl ester

Product 1

HCID 68614494HCID 68614494, compound

Procedure

In an analogous manner to that described in Example 28b), the alkylation of the (R)-1-(4-hydroxy-phenyl)-5-oxo-pyrrolidine-3-carboxylic acid methyl ester [Example 28a)] with 3-chlorobenzylalcohol yields the (R)-1-[4-(3-chloro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid methyl ester as a white solid. MS: m/e=360 (M+H)+.

Sources & evidence

ORD record
ord-3789e6e688a644b593c42195c6bdfcd5
Source dataset
uspto-grants-2006_05
Patent number
US07037935B2

Reaction notes

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