HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → L-Alanine 1,1-dimethylethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl (R)-2-[(trifluoromethylsulfonyl)oxy]propionate | HCID 13563137 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | L-Alanine 1,1-dimethylethyl ester | HCID 89016 | — |
Reaction Steps
To a solution of 4-nitrophenylalanine, ethylester, hydrochloride (2.3 g) in dichloromethane (10 ml), add triethylamine (2.55 ml) and then t-butyl 2(R)-(trifluoromethanesulfonyloxy)propionate (2.80 g) (see Preparation 4) in dichloromethane (10 ml). Stir the resulting solution at room temperature for 20 hours. Concentrate the reaction mixture, add diethyl ether and extract with salt solution. Dry over magnesium sulfate and concentrate the ether solution in vacuo to give an oil. Place the oil on a column of silica gel (100 ml, 60-200 mesh) and elute with diethyl ether:hexane 60:40 to give N-[1(S)-ethoxycarbonyl)-2-(4-nitrophenyl)ethyl]-(S)-alanine, t-butyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04584285 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-ea07f7a212ce450e91e9d510405096ee |
| Source note | uspto-grants-1986_04 |