HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419535Generated: October 25, 2026
Hydrochloric Acid → 2-(2-Iminothiazolidin-3-yl)-1-phenylethanol hydrochloride
https://huagongshe.com/reaction/2419535
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thiocyanic Acid | HCID 781 | — |
| Reactant | Aziridine | HCID 9033 | — |
| Reactant | 1-Aziridineethanol, alpha-phenyl- | HCID 28834 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2-Iminothiazolidin-3-yl)-1-phenylethanol hydrochloride | HCID 2723670 | — |
Reaction Steps
To the stirred solution of thiocyanic acid is added a solution of the crude dl-α-phenyl-1-aziridineethanol in 250 ml. of ethanol at a rate sufficient to keep the reaction temperature at 30°-35° C. After the aziridine addition is complete, 72 g. of a methanolic solution of hydrogen chloride (0.35 mole) is added and the solution stirred for 1.5 hours at room temperature. An additional 0.05 mole of hydrogen chloride in 10 g. of ethanol is added, and the reaction heated at 35°-40° C. for 0.5 hour. It is then allowed to proceed at room temperature for 2.5 days. The mixture is concentrated under reduced pressure to about 100 ml., filtered, washed with ethanol and dried to give 27.1 g. of white crystals, melting point 198°-200° C. The yield is 42% (based on styrene oxide) or 71% (based on dl-α-phenyl-1-aziridineethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04107170 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-509eae68885e48feb04f133ddc92a662 |
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| Source note | uspto-grants-1978_08 |
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