HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → O-methoxymethyl-N-methyl-beta-benzoyloxytyrosine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-beta-benzoyloxytyrosine methyl ester | HCID 54000197 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | O-methoxymethyl-N-methyl-beta-benzoyloxytyrosine methyl ester | HCID 53867281 | 9.1% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05217952 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-84a406341554443b9bcd9ed4c5e779d9 |
| Source note | uspto-grants-1993_06 |