HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → 4-Amino-N-propoxy-2,2,6,6-tetramethylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | N-Propoxy-4-oxo-2,2,6,6-tetramethylpiperidine | HCID 23450603 | — |
| Product | 4-Amino-N-propoxy-2,2,6,6-tetramethylpiperidine | HCID 23450599 | 62% |
Reaction Steps
4-Amino-N-propoxy-2,2,6,6-tetramethylpiperidine (1.6 g, 62%) is prepared from N-propoxy-4-oxo-2,2,6,6-tetramethylpiperidine (12.2 mmol, 2.60 g) by the same method as described above, with the exception of the addition of ammonium acetate (122 mmol, 9.40 g), 6 g molecular sieves (10−10 m) and 95% NaBH3CN (12.2 mmol, 0.8 g). 1H-NMR (CDCl3); δ=3.61 (t, J=6.6 Hz, 2H, CH2—O), 2.99 (m, 1H, NH2—CH), 1.58 (d, J=11.4 Hz, 2H, NH2), 1.46 (m, 2H, CH2—CH3), 1.20 (m, 4H), 1.16 (s, 6H, CH3), 1.13 (s, 6H, CH3), 0.93 (t, J=7.4 Hz, 3H, CH2—CH3); 13C-NMR (CDCl3): δ=78.3, 59.8, 49.9, 41.4, 33.2, 21.9, 20.9, 10.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247479B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-89b46945bd04428c872bcdbe320998f3 |
| Source note | uspto-grants-2012_08 |