HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenethylamine → N-((1R)-1-Phenylethyl)glycine ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenethylamine | HCID 7408 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-((1R)-1-Phenylethyl)glycine ethyl ester | HCID 6455333 | 63% |
Reaction Steps
Ethyl bromoacetate (4.14 g; 24.8 mmol) was treated with (R) α-methylbenzylamine (3 g, 24.8 mmol) and ethyldiisopropylamine (3.2 g; 24.8 mmol) in toluene (100 mL). After heating at reflux for 18 hours, the mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by flash chromatography (SiO2, 20% ethyl acetate/pentane) to provide the title compound (3.2 g, 63% yield). MS (DCI/NH3) m/z 208 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119635B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-5eedbaa1ab04496a94960ab181062da5 |
| Source note | uspto-grants-2012_02 |