HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Phenylalanine → HCID 11069180, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Ethanol, 2-(phenylseleno)- | HCID 11030856 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11069180 | HCID 11069180 | — |
Reaction Steps
In a 50 ml round bottomed flask, 2.55 g (13.3 mmol) of 1-(3-dimethylamino propyl)-3-ethyl carbodiimide hydrochloride and 1.7 g of (8.2 mmol) phenylalanine were added to a solution of 1.87 g (9.3 mmol) of 2-(phenylseleno)ethanol in 20 ml of THF. The reaction mixture was then stirred for 12 hours at room temperature. The mixture was then diluted with 50 ml of ethyl acetate and extracted with 50 ml of a 0.5 M HCl solution. The organic phase was dried over sodium sulfate, filtered, and the solvent was removed in vacuo. Purification by column chromatography (PE:EE=2:1) yielded 2.9 g (91% of th., 98% of lit.) of a yellowish liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08999323B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-6f795c9c7dd7420494421229fb03b2f9 |
| Source note | uspto-grants-2015_04 |