Methyl morpholine oxide → 4-Formyl-2-phenylbenzoyl methionine methyl ester

HRID 2121123Notes

Reaction equation

HRID 2121123 reaction equation
[CH3:1][O:2][C:3](=[O:26])[C@H:4]([CH2:22][CH2:23][S:24][CH3:25])[NH:5][C:6](=[O:21])[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][OH:14])=[CH:9][C:8]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.C[N+]1([O-])CCOCC1.C(Cl)Cl.C(#N)C>C(OCC)C.CCC[N+](CCC)(CCC)CCC.[O-][Ru](=O)(=O)=O>[CH3:1][O:2][C:3](=[O:26])[C@H:4]([CH2:22][CH2:23][S:24][CH3:25])[NH:5][C:6](=[O:21])[C:7]1[CH:12]=[CH:11][C:10]([CH:13]=[O:14])=[CH:9][C:8]=1[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1

Participants

6

Procedure

A mixture of the resultant alcohol from Example 16D (1.0 equivalent), N-methylmorpholine-N-oxide (1.5 equivalents), molecular sieves, and a catalytic amount of TPAP is stirred in a CH2Cl2/acetonitrile mixture until the reaction is judged complete by TLC analysis. The mixture is diluted with ethyl ether and filtered through SiO2. The product is purified by chromatography on silica gel.

Workup

  1. filtrationfiltered through SiO2
  2. customThe product is purified by chromatography on silica gel

Sources & evidence

ORD record
ord-5fec34a6cc6c405fad4872d42bc2fe27
Source dataset
uspto-grants-2004_02
Patent number
US06693123B2

Reaction notes

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