HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → tert-Butyl [3-(benzyloxy)cyclobutyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(Benzyloxy)cyclobutane-1-carboxylic acid | HCID 12815111 | — |
| Reactant | Phosphoric acid diphenylester azide | HCID 66782931 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl [3-(benzyloxy)cyclobutyl]carbamate | HCID 53415284 | — |
Reaction Steps
9.28 g (45 mmol) 3-benzyloxy-cyclobutancarboxylic acid (Org. Lett. 6(11), 1853-1856, 2004) are suspended in 80 ml dry tert-butanol and combined with 5.1 g (50 mmol) triethylamine and 13.8 g (50 mmol) phosphoric acid diphenylester azide. The reaction mixture is stirred for 20 h under reflux conditions. The solvent is eliminated in vacuo and the residue is taken up in dichloromethane. The organic phase is washed three times with 2 N sodium hydroxide solution, dried with sodium sulphate and the dichloromethane is eliminated in vacuo. The crude product is recrystallised from acetonitrile (1 g crude product: 5 ml acetonitrile).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07521457B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-87a78f87589549f787aa886342058bac |
| Source note | uspto-grants-2009_04 |