HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733802Generated: October 27, 2026
Hydrochloric Acid → 2-(2-Aminoethylthio)thioxanthone
https://huagongshe.com/reaction/1733802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Reactant | 2-Chlorothioxanthone | HCID 618848 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2-Aminoethylthio)thioxanthone | HCID 18939133 | — |
Reaction Steps
17.0 g. (0.15 mol) of cysteaminium chloride and 19.8 g. (0.3 mol) of potassium hydroxide are boiled for 3 hours on a water separator in 180 ml. of toluene. 24.6 g. (0.1 mol) of 2-chlorothioxanthone and 180 mol of dimethylpropyleneurea are added to the evaporated residue, and the mixture is stirred for 20 hours at 100° C. The reaction mixture is poured into 1 l of 2N hydrochloric acid and the aqueous phase is extracted with ethyl acetate. The aqueous phase then adjusted to pH 10 and extracted with ethyl acetate. Work-up of the organic phase gives 24.0 g. of the analytically pure compound IIIb.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05532112 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-a909326bd4ba482d89bb475fc49938d7 |
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| Source note | uspto-grants-1996_07 |
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