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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580783Generated: October 25, 2026

Hydrochloric Acid → N-(2-hydroxy-3-dodecyloxy)propyl-L-arginine hydrochloride

https://huagongshe.com/reaction/580783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropanolHCID 3776—
Reactant1-Dodecyl glycidyl etherHCID 17163—
ReactantHCID 178418600HCID 178418600—
SolventWaterHCID 962—
ProductN-(2-hydroxy-3-dodecyloxy)propyl-L-arginine hydrochlorideHCID 17844343236%

Reaction Steps

L-arginine (17.4 g, 0.1 mols) was dissolved in 100 ml of water in a three-necked round flask, and 100 ml of i-propanol were added thereto. Then, 24.2 g (0.1 mols) of dodecylglycidyl ether (made by Sakamoto Yakuhin Kogyo Co., Ltd.) were added dropwise thereto over a period of 30 minutes while being heat-refluxed and stirred. Further, the mixture was stirred under reflux for 3 hours. It was determined through TLC and gas chromatography that dodecylglycidyl ether disappeared. Thereafter, the resulting mixture was neutralized with 10.1 g (0.1 mols) of 36% hydrochloric acid. The reaction solution was concentrated under reduced pressure, and the residue was purified through silica-gel column chromatography (Kieselgel 60 made by Merck & Co., Inc., eluent=mixture of chloroform, methanol and acetic acid at a ratio of 3:1:0.5) to give 15.0 g of N-(2-hydroxy-3-dodecyloxy)propyl-L-arginine hydrochloride (yield 36.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919748
Source datasetuspto-grants-1999_07
ORD IDord-686539c3e530471ea9f28bac0c5cbb0e
Source noteuspto-grants-1999_07