HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → N-t-butyldimethylsilyloxycarbonylvaline 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 | N-(tert-Butoxycarbonyl)-L-valine methyl ester | HCID 11031717 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-t-butyldimethylsilyloxycarbonylvaline methyl ester | HCID 13934325 | — |
Reaction Steps
To a methylene chloride solution (1.0 ml) of N-t-butoxycarbonyl-L-valine methyl ester (115.5 mg, 0.5 mmol) and 2,6-lutidine (0.116 ml, 1.0 mmol) was added dropwise t-butyldimethylsilyltrifluoromethane sulfonate (0.172 ml, 0.75 mmol) 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 153.2 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04837349 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-b943ef89acb54ada8861d8394caf3533 |
| Source note | uspto-grants-1989_06 |