Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86638633 | HCID 86638633 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 55284693 | HCID 55284693 | — |
Reaction Steps
To a solution of tert-butyl (R)-1-((R)-tetrahydrofuran-2-yl)propylcarbamate (2.67 g, 11.64 mmol) in 1,4-dioxane (80 ml) was added 5M HCl (5 ml). The reaction was then heated at 70° C. for 5.5 hours and after cooling to RT, the mixture was concentrated in vacuo to afford the title compound; 1H NMR (MeOD) δ1.09 (3H, t, CH3), 1.7 (3H, m), 2.0 (2H, m), 2.15 (1H, m), 3.0 (1H, m), 3.88 (3H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07989497B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-92a7d7c95bf64058bb0f0e43be307094 |
|---|
| Source note | uspto-grants-2011_08 |
|---|