HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → di-tert-butyl (2,3,4,5-tetrafluorobenzoyl)-L-glutamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Di-tert-butyl glutamate hydrochloride | HCID 208636 | — |
| Reactant | 2,3,4,5-Tetrafluorobenzoyl chloride | HCID 2733689 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | di-tert-butyl (2,3,4,5-tetrafluorobenzoyl)-L-glutamate | HCID 11270493 | — |
Reaction Steps
To an ice-cold solution of di-tert-butyl L-glutamate hydrochloride (6.6 g, 22.4 mmol) and Et3N (6.9 ml, 50 mmol) in dry CH2Cl2 (70 ml) was added, over a period of 1.5 hr, 2,3,4,5-tetrafluorobenzoyl chloride (5.0 g, 23.5 mmol) in dry CH2Cl2 (20 ml) and thirty minutes later the solution was allowed to warm to room temperature. Sixteen hours later the solution was washed with H2O, dried (MgSO4) and evaporated to dryness. 1H NMR δ 1.40+1.42 (2s, 18H, t-butyl), 1.85+1.95 (2m, 2H, CH2CH), 2.34 (t, 2H, CH2CO, J=7.5 Hz), 4.3 (m, 1H, CH), 7.57 (m, 1H, H6), 8.80 (d, 1H, NH, J=7.5 Hz); 19F NMR δ −138.6+139.0 (2m, 2F, F2+5), −152.4 (m, 1H, F4), −154.9 (t, 1F, F3, J=20 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852755B1 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-b2e52de445c646f1a9a2145db1d992a4 |
| Source note | uspto-grants-2005_02 |