HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619003Generated: October 25, 2026
Hydrochloric Acid → HCID 178443282, compound
https://huagongshe.com/reaction/619003
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 1-Dodecyl glycidyl ether | HCID 17163 | — |
| Reactant | HCID 178418600 | HCID 178418600 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178443282 | HCID 178443282 | 36% |
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 identified 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-dodecyloxypropyl)-L-arginine hydrochloride (yield 36.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05958869 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-254aae6cdc7e4c2c8f67f090335487b3 |
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| Source note | uspto-grants-1999_09 |
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