HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108003Generated: October 26, 2026
Acetic Acid → 3-Phenylmethyl-2-thiazolidinone
https://huagongshe.com/reaction/2108003
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-Imino-3-phenylmethylthiazolidine hydrobromide | HCID 23045100 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Phenylmethyl-2-thiazolidinone | HCID 10921389 | 42.3% |
Reaction Steps
To a solution of 2.73 g (0.01 mol) of 2-imino-3-phenylmethylthiazolidine hydrobromide in 10 ml of water 1.36 g of anhydrous sodium acetate and 0.62 ml of glacial acetic acid are added, then 0.75 g of sodium nitrite dissolved in 3 ml of water is dropped to the above mixture at 5° C. under stirring, then the mixture is stirred at 5° C. for additional 3 hours. After standing in a refrigerator overnight, the solution is stirred at room temperature for 3 hours. After rubbing, a precipitate appears which is filtered off, washed with water, dried and then refluxed with five volumes of n-butanol for 2 hours. After evaporating the solvent, the residue is thoroughly rubbed with diisopropyl ether and the product is filtered off. Thus, 0,81 g (42.3%) of the title product is obtained, m.p.: 49°-50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04937252 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-f980a061cec643779b9e33f8bd6ecc4e |
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| Source note | uspto-grants-1990_06 |
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