HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (S)-4-(4-Fluorobenzyl)oxazolidine-2,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | N-(tert-Butoxycarbonyl)-4-fluoro-L-phenylalanine | HCID 7020910 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-4-(4-Fluorobenzyl)oxazolidine-2,5-dione | HCID 59753664 | — |
Reaction Steps
To a solution of 2(S)-tert-butoxycarbonylamino-3-(4-fluorophenyl)propionic acid (1.5 g, 5.29 mmol) in ethyl acetate (100 mL) under an argon atmosphere was added triphosgene (628 mg, 2.12 mmol). To the solution was added triethylamine (0.8 mL 5.76 mmol,) over 1 min, and the reaction stirred for 72 h at rt. The reaction mixture was filtered, and the filtrate concentrated in vacuo to yield an oily residue. The crude material was crystallised from cold dichloromethane and petroleum ether to give the title compound. δH (CD3OD): 7.20 (2H, m), 7.10 (2H, m), 5.86 (1H, s, (NH)), 4.58 (1H, s), 3.33–3.23 (2H, m), 3.11–3.00 (1H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07405210B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-b5521b9e8fce4ff29543c84c4e48f37b |
| Source note | uspto-grants-2008_07 |