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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185684Generated: October 30, 2026

Triethylamine → HCID 131723263, compound

https://huagongshe.com/reaction/2185684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
Reactant(2S)-2-(((Phenylmethoxy)carbonyl)amino)butanoic acidHCID 7349998—
ReactantHCID 77752115HCID 77752115—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 131723263HCID 131723263—

Reaction Conditions

Temperature0 °C

Reaction Steps

3,3-Dimethylindoline-2(R/S)-carboxylic acid butylamide (1.000 g, 4.08 mmol) and N-benzyloxycarbonyl-2(S)-aminobutyric acid (1.451 g, 6.12 mmol) were dissolved in dry tetrahydrofuran (25 ml). The solution was cooled to 0° C. and triethylamine (2.44 ml, 13.78 mmol) and bis(2-oxo-3-oxazolidinyl)phosphinyl chloride (2.338 g, 9.183 mmol) were added. The mixture was stirred at room temperature for 22 hours and ethyl acetate (40 ml) was then added, and the mixture was washed with 3N hydrochloric acid (3×50 ml), 5% sodium bicarbonate (3×50 ml) and water (50 ml) and dried over sodium sulphate. After removing the solvent, several successive purifications by chromatography on a column of silica gel gave the product in the form of an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403561B1
Source datasetuspto-grants-2002_06
ORD IDord-f36c178a9da14e7bb913f65532606823
Source noteuspto-grants-2002_06