HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371867Generated: November 3, 2026
2-Methylthiazolidine → HCID 19905282, compound
https://huagongshe.com/reaction/2371867
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylthiazolidine | HCID 32196 | — |
| Reactant | 2-Chloro-4'-fluoropropiophenone | HCID 67672 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19905282 | HCID 19905282 | 84.1% |
Reaction Steps
3.73 g (0.02 mol) of β-chloro-4-fluoropropiophenone are added in little portions at room temperature to a suspension containing 2.06 g (0.02 mol) of 2-methylthiazolidine and 1.64 g (0.02 mol) of anhydrous sodium acetate in 20 ml of ethanol over 30 minutes under stirring. After stirring for an additional 3 hours, the reaction mixture is evaporated, saturated sodium hydrogen carbonate solution is added to the oily yellow residue and it is extracted twice with 30 ml of ether each. After drying and evaporating the extract, the oily yellow residue is dissolved in acetone and acidified by 48% hydrobromic acid. Thus, 4.26 g of a white crystalline product are obtained and recrystallized twice from ethanol to give 2.00 g (29.9%) of hydrobromide of the title compound, m.p.: 151°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05096902 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-cef2e62477e64803843e1171c57e1ad6 |
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| Source note | uspto-grants-1992_03 |
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