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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266968Generated: October 31, 2026

Triethylamine → HCID 11122265, compound

https://huagongshe.com/reaction/1266968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 10970796HCID 10970796—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
ProductHCID 11122265HCID 1112226567%

Reaction Steps

N-(4-Fluorophenylsulfonyl)-D-valyl-D-leucinol (1.5 g) was dissolved in dimethyl sulfoxide (20 ml) and dichloromethane (10 ml), and triethylamine (2.4 g) was added. The solution was stirred at room temperature while adding a solution (20 ml) of sulfur trioxide-pyridine complex (2.6 g) in dimethyl sulfoxide, which was followed by stirring for 1 hr. After the completion of the reaction, ethyl acetate was added. The mixture was washed with dilute hydrochloric acid, saturated aqueous solution of sodium hydrogencarbonate and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by preparative TLC plate (developing solvent: hexane-ethyl acetate, 1:1, v/v) to give 1.0 g of N-(4-fluorophenylsulfonyl)-D-valyl-D-leucinal (Compound 55) as white crystals. [Step 1]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06551999B1
Source datasetuspto-grants-2003_04
ORD IDord-33e7aa2018e24e7e9727395c5524e6fb
Source noteuspto-grants-2003_04