HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → HCID 14765842, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyldimethylsilyl trifluoromethanesulphonate | HCID 123564 | — |
| Reactant | N-Boc-allylglycine methyl ester | HCID 22243128 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14765842 | HCID 14765842 | — |
Reaction Steps
To a methylene chloride solution (1.5 ml) of N-(t-butoxycarbonyl)-allylglycine methyl ester (183 mg, 0.8 mmol) and 2,6-lutidine (0.186 ml, 1.6 mmol) was added t-butyldimethylsilyltrifluoromethane sulfonate (TBDMSOTf) (0.275 ml, 1.2 mmol) at room temperature in a nitrogen atmosphere. After the mixture was stirred for 15 minutes, a saturated aqueous solution of ammonium chloride (3 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 260 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04837349 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-9ddae1b29bce4278a1064e3de9d1ce72 |
| Source note | uspto-grants-1989_06 |