Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibenzylamine | HCID 7656 | — |
| Reactant | (S)-3-(2-Amino-3-nitrophenoxy)-1,2-epoxypropane | HCID 15049327 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54232526 | HCID 54232526 | 78% |
Reaction Steps
(S)-3-(2-Amino-3-nitrophenoxy)-1,2-epoxypropane (8.0 g, 38.1 mmol) was dissolved in 250 mL of methanol and treated with dibenzylamine (8.05 mL, 42.0 mmol, d=1.026). The mixture was stirred at reflux for 10 hours and then cooled to 0° C. The resulting orange precipitate was filtered and washed with cold methanol, then dried to yield 12.1 g (78%) of a pale orange solid that was pure by NMR and TLC analysis. The material was used without further purification. NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06060492 |
|---|
| Source dataset | uspto-grants-2000_05 |
|---|
| ORD ID | ord-3615c9658aed4847b1309781728d7424 |
|---|
| Source note | uspto-grants-2000_05 |
|---|