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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373392Generated: October 27, 2026

Citric Acid → HCID 14336499, compound

https://huagongshe.com/reaction/373392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBOC-D-LEU-OH H2OHCID 2724763—
ReactantO-benzyl-L-valine toluene-p-sulphonateHCID 11567066—
ReactantHCID 18959840HCID 18959840—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 14336499HCID 14336499110.2%

Reaction Steps

0.749 g (3.00 mmol) of Boc-D-leucine monohydrate, 1.252 g (3.30 mmol) of L-valine benzyl ester p-toluenesulfonate and 0.811 g (6.00 mmol) of N-hydroxybenzotriazole were dissolved in 15 ml of dichloromethane. The resulting mixture was cooled with ice, and admixed with 0.504 ml (3.60 mmol) of triethylamine and 1.108 g (4.20 mmol) of 97% 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide perchlorate. The reaction mixture was stirred for 2 hours, and then further stirred at room temperature for 4 hours. After the completion of the reaction, 30 ml of water and 5 ml of a 1% aqueous citric acid solution were added to the reaction mixture. The crystals thus deposited were filtered off. The organic layer successively was washed with 20 ml of water, 20 ml of a saturated aqueous sodium hydrogen carbonate solution and 10 ml of water, dried over anhydrous sodium sulfate, and distilled to remove the solvent therefrom, whereby 1.390 g of crude Boc-D-leucyl-L-valine benzyl ester product were obtained as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162500
Source datasetuspto-grants-1992_11
ORD IDord-c2907bbe056e4674bccabd51ce6b7734
Source noteuspto-grants-1992_11