HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminopyridine → Dodecyl carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dodecyl chloroformate | HCID 90513 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Dodecyl carbamate | HCID 233116 | 120.3% |
Reaction Steps
To a solution of 4-aminopyridine (3.00 g, 31.9 mmol) in CH2Cl2 (50 mL) at 0° C. was added triethylamine (5.60 mL, 40.0 mmol) and dodecyl chloroformate (8.70 g, 35.0 mmol). The ice bath was removed and the resulting mixture was allowed to warm to rt over 3 h before being poured into saturated aqueous NaHCO3. The product was extracted with CH2Cl2, washed with brine, dried (MgSO4) and concentrated. The crude product was recrystallized from EtOAc/hexanes to give 8.80 g (90% yield) of pure dodecyl carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08729107B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-859e2e30968645fc9d791f2f7c034b95 |
| Source note | uspto-grants-2014_05 |