HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → N-(t-Butyldimethylsilyloxycarbonyl)-L-methionine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyldimethylsilyl trifluoromethanesulphonate | HCID 123564 | — |
| Reactant | (S)-Methyl 2-((tert-butoxycarbonyl)amino)-4-(methylthio)butanoate | HCID 11097398 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(t-Butyldimethylsilyloxycarbonyl)-L-methionine methyl ester | HCID 13934327 | — |
Reaction Steps
To a methylene chloride solution (1.0 ml) of N-t-butoxycarbonyl-L-methionine methyl ester (131.5 mg, 0.5 mmol) and 2,6-lutidine (0.116 ml, 1.0 mmol), t-butyldimethylsilyltrifluoromethane sulfonate (TBDMSOTf) (0.172 ml, 0.75 mmol) was added dropwise at room temperature in a nitrogen atmosphere. After the mixture was stirred for 15 minutes, a saturated aqueous solution of ammonium chloride (2 ml) was added to quench the reaction and extraction with ether was conducted. The organic layer was dried over anhydrous magnesium sulfate and filtered. By distilling off the solvent under vacuum, the titled compound was obtained in an amount of 146 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04837349 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-54293b7aebdf400ea2dde9437087daa5 |
| Source note | uspto-grants-1989_06 |