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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411959Generated: October 31, 2026

Hydrochloric Acid → HCID 178443806, compound

https://huagongshe.com/reaction/411959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 11096866HCID 11096866—
ReactantHCID 11810633HCID 11810633—
ReactantHCID 178419078HCID 178419078—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 178443806HCID 17844380663%

Reaction Conditions

Temperature250 °C

Reaction Steps

30 g of N-octyloxycarbonyl-β-alanine were dissolved in 300 ml of dimethylformamide and 1 molar equivalent of triethylamine. Next, 1 molar equivalent of 2-(5-norbornene-2,3-dicarboximido)-1,1,3,3-tetramethyluronium tetrafluoroborate was added. The mixture was then stirred for 1 hour at a temperature of 250° C. Next, a solution containing 1.2 molar equivalents of histidine and 1.2 molar equivalents of sodium hydroxide in 100 ml of water were added dropwise, while keeping the temperature below 30° C. After stirring for 6 hours, the mixture was neutralized with 1 molar equivalent of 5N hydrochloric acid, followed by 100 ml of water. After stirring for 30 minutes, the mixture was poured into 2 liters of acetone. The white precipitate formed was filtered off and dried. The crude product was dissolved in 10 ml/g of refluxing 96% ethanol. The solution was filtered while hot and the product then crystallized at room temperature. After processing the precipitate, 29.4 g of a white crystalline product were obtained (63% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562789B2
Source datasetuspto-grants-2003_05
ORD IDord-d066212d4a474289a0f83265b12131af
Source noteuspto-grants-2003_05