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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23610Generated: October 25, 2026

Triethylamine → di-tert-butyl (2,3,4,5-tetrafluorobenzoyl)-L-glutamate

https://huagongshe.com/reaction/23610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDi-tert-butyl glutamate hydrochlorideHCID 208636—
Reactant2,3,4,5-Tetrafluorobenzoyl chlorideHCID 2733689—
SolventDichloromethaneHCID 6344—
Productdi-tert-butyl (2,3,4,5-tetrafluorobenzoyl)-L-glutamateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852755B1
Source datasetuspto-grants-2005_02
ORD IDord-b2e52de445c646f1a9a2145db1d992a4
Source noteuspto-grants-2005_02