HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-[(Benzyloxy)methyl]-1-tritylaziridine → 2-[(Benzyloxy)methyl]aziridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-[(Benzyloxy)methyl]-1-tritylaziridine | HCID 78156232 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Triethylsilane | HCID 12052 | — |
| Product | 2-[(Benzyloxy)methyl]aziridine | HCID 86602786 | — |
Reaction Steps
To a cold (0° C.) solution of 2-[(benzyloxy)methyl]-1-tritylaziridine (1.28 g, 3.16 mmol) in dichloromethane (13 mL), trifluoroacetic acid (1 mL) and triethylsilane (2.0 mL) was added and stirred at the temperature for 1 h. The resultant mixture was concentrated under vacuum, and the residue was partitioned between ether and brine. The organic extract was dried with anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with a mixture of 50-100% THF in hexane. Collection and concentration of appropriate fractions provided 2-[(benzyloxy)methyl]aziridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07517532B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-22c1b535cf6d413b91a75cd5230e7cd9 |
| Source note | uspto-grants-2009_04 |