HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703381Generated: October 26, 2026
Hydrochloric Acid → 8-Guanidino-3-hydroxyoctanamide hydrochloride
https://huagongshe.com/reaction/703381
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Bis(S-methylisothiouronium) sulfate | HCID 13347 | — |
| Reactant | 8-Amino-3-hydroxyoctanamide hydrochloride | HCID 22149892 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 8-Guanidino-3-hydroxyoctanamide hydrochloride | HCID 178479437 | 113.3% |
Reaction Steps
To a solution of 670 mg of 8-amino-3-hydroxyoctanamide hydrochloride in 8 ml of 1N aqueous sodium hydroxide solution, was added 668 mg (2.4 mmoles) of S-methylisothiourea hemisulfate. The mixture was stirred overnight at room temperature. The reaction mixture was adjusted to pH 6 with 1N hydrochloric acid, evaporated to dryness and dissolved in 5 ml of 1M saline. The solution was passed through a column of 160 ml of Diaion® HP-20 (Mitsubishi Chemical Co.) and the column was eluted successively with 400 ml of 1M saline, 400 ml of 0.8M saline and 800 ml of 0.6M saline (15 g fraction size). Fractions No. 41 to No. 87 were combined, evaporated to dryness and extracted three times with 10 ml of methanol. The methanol layer was passed through a column of 300 ml of Sephadex® LH-20 and eluted with methanol to effect desalting (7 ml fraction size). Fractions No. 25 to 35 were combined and evaporated to dryness to obtain 687 mg (85% yield) of 8-guanidino-3-hydroxyoctanamide hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983328 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-f2b4734004ab4c58ad96b10615fa51ff |
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| Source note | uspto-grants-1991_01 |
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