HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058639Generated: October 29, 2026
3,4-Dichlorophenylacetic acid → HCID 85074710, compound
https://huagongshe.com/reaction/1058639
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dichlorophenylacetic acid | HCID 79874 | — |
| Reactant | HCID 178518521 | HCID 178518521 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 85074710 | HCID 85074710 | — |
Reaction Steps
3,4-Dichlorophenylacetic acid was dissolved in SO2Cl2 followed by addition of a few drops of DMF. This resulting mixture was heated to 80 ° C for 15-30 min. followed by concentration of the reaction mixture under reduced pressure. The residue was dissolved in THF and slowly added to a solution of 5-(hydroxybenzylidene)thiazolidine-2,4-dione (1.5 eq.) and TEA (1.5 eq.) in THF. The resulting reaction was stirred for 1-2 h at which time the solid was filtered off and filtrate was concentrated under reduced pressure to yield light yellow solid. The solid was dissolved in EtOAc followed by washing with sat. aq. K2CO3. The organic phase was separated, and dried over Na2SO4 followed by concentration under reduced pressure to yield pure compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518268B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-e76cf67aca35445690d7136439dc1666 |
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| Source note | uspto-grants-2003_02 |
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