HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → benzyl N-pyridin-3-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Aminopyridine | HCID 10009 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | benzyl N-pyridin-3-ylcarbamate | HCID 4323589 | 39.3% |
Reaction Steps
To a solution of 3-aminopyridine (10 g, 0.106 mol) and triethyl amine (16.3 mL, 0.117 mol) in dichloromethane (100 mL) at 0° C., was added benzyl chloroformate (15.2 mL, 0.106 mol) slowly. The reaction mixture was stirred overnight and was washed with water, saturated NaHCO3, dried over MgSO4, and evaporated. The residue was purified on a silica gel column to give the product (9.51 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05492916 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-21302e956b554cc7913f7c0fb9fb4cf0 |
| Source note | uspto-grants-1996_02 |