Trifluoroacetic acid → O-methoxymethyl-N-methyl-beta-benzoyloxytyrosine methyl ester

HRID 1587286Notes

Reaction equation

HRID 1587286 reaction equation
[CH3:1][O:2][C:3](=[O:37])[C@H:4]([CH:17]([O:28][C:29](=[O:36])[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[C:18]1[CH:23]=[CH:22][C:21]([O:24][CH2:25][O:26][CH3:27])=[CH:20][CH:19]=1)[N:5]([CH3:16])SC1C=CC=CC=1[N+]([O-])=O.C1(S)C=CC=CC=1.FC(F)(F)C(O)=O.C(=O)(O)[O-].[Na+]>ClCCl>[CH3:1][O:2][C:3](=[O:37])[C@H:4]([CH:17]([O:28][C:29](=[O:36])[C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1)[C:18]1[CH:23]=[CH:22][C:21]([O:24][CH2:25][O:26][CH3:27])=[CH:20][CH:19]=1)[NH:5][CH3:16]

Participants

6

Procedure

To a solution of O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-β-benzoyloxytyrosine methyl ester (threo isomer) (4.94 g) in dichloromethane (50 ml) were added thiophenol (4.8 ml) and trifluoroacetic acid (2.5 ml) at 0° C. After stirring for 30 minutes, sodium bicarbonate aqueous solution was added to the mixture. The organic layer was washed with sodium bicarbonate aqueous solution and brine. After evaporating, the residue was put on a column of silica gel (MERCK 7734, 100 g) and eluted with 5% methanol in chloroform to give O-methoxymethyl-N-methyl-β-benzoyloxytyrosine methyl ester (threo isomer) (0.32 g).

Workup

  1. washThe organic layer was washed with sodium bicarbonate aqueous solution and brine
  2. customAfter evaporating
  3. washeluted with 5% methanol in chloroform

Sources & evidence

ORD record
ord-84a406341554443b9bcd9ed4c5e779d9
Source dataset
uspto-grants-1993_06
Patent number
US05217952

Reaction notes

Loading…