HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Tert-butyl 2-(cyclobutylamino)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclobutylamine | HCID 75645 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Product | Tert-butyl 2-(cyclobutylamino)acetate | HCID 20285462 | 67.2% |
Reaction Steps
An ethanolic solution of t-butyl bromoacetate (39 g, 0.2 mol) was added dropwise to a stirred chilled ethanolic solution containing cyclobutyl amine (28.4 g, 0.4 mol) and triethylamine (25.3 g, 0.25 mol). After stirring overnight at room temperature, the reaction mixture was concentrated and the residue redissolved in methylene chloride (300 ml). This solution was washed with water (3×500 ml), dried over MgSO4, filtered, and evaporated to dryness, yielding 24.9 g (67%) of the desired product as a light brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256761 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-a763cbe104794b3dae93b8f44f1c68ab |
| Source note | uspto-grants-1981_03 |