HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentylamine → Tert-butyl 2-(cyclopentylamino)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Tert-butyl 2-(cyclopentylamino)acetate | HCID 13298943 | 66% |
Reaction Steps
To a chilled (0°-5° C.) and stirred ethereal solution (500 ml) containing cyclopentyl amine (75 g, 0.88 mol) and triethyl amine (101 g, 1.0 mol) was added t-butyl bromoacetate (136.5 g, 0.7 mol) in ether (300 ml). The reaction mixture was stirred overnight. The ethereal mixture was then concentrated and the residue redissolved in methylene chloride (750 ml). This solution was washed with saturated aqueous sodium bicarbonate (1000 ml), water (2×3000 ml), and brine (2000 ml). The organic portion was separated, dried over MgSO4, filtered and evaporated yielding N-cyclopentylglycine t-butyl ester (92 g, 66%) as a brown oil which slowly crystallized on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256761 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-19059f66fe404d81bba0e4a7822a2b75 |
| Source note | uspto-grants-1981_03 |