HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 3-(Benzyloxycarbonylamino)-1-propoxyamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-(Benzyloxycarbonylamino)-1-propoxylphthalimide | HCID 131722634 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Benzyloxycarbonylamino)-1-propoxyamine | HCID 11775796 | 97% |
Reaction Steps
To a solution of N-[3-(benzyloxycarbonylamino)-1-propoxylphthalimide (1.42 g, 4.0 mmol), as prepared in the preceding step, in ethanol (20 mL) and tetrahydrofuran (20 mL) was added 40% methylamine (2 mL, 25 mmol). The solution was stirred at room temperature for 1 h. The solvent was evaporated and the residue passed through silica gel (3:1 ethyl acetate:hexane to ethyl acetate) to give the title compound as a white solid (870 mg, 97%). 1H-NMR (300 MHz, CDCl3) δ7.36 (m, 5H), 5.38 (br s, 2H), 5.09 (s, 2H), 5.08 (br s, 1H), 3.73 (t, J=5.9 Hz, 2H), 3.29 (q, J=6.2 Hz, 2H), 1.79 (pentet, J=6.2 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706021B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-5738fd1b045e4fd6befaf6c1d7d5c5d6 |
| Source note | uspto-grants-2004_03 |