HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476769Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 86743551, compound
https://huagongshe.com/reaction/476769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 2-Butanamine, 2-methyl- | HCID 68986 | — |
| Reactant | Dimethyl tetrafluorophthalate | HCID 616675 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86743551 | HCID 86743551 | — |
Reaction Steps
3,4,5,6-Tetrafluoro-1,2-benzenedicarboxylic acid, dimethyl ester (Example 1), 2.66 g, is treated with 8 g of dimethylsulfoxide and the mixture is warmed to dissolve the solid. The solution is cooled in an ice bath and 2.65 g of tertiary-pentylamine is added. The resulting solution is then stirred at room temperature for three hours, 50 ml of water added, and the solution extracted with heptanes (2×30 ml). The combined heptane extract is extracted with a 5% aqueous solution of hydrochloric acid (2×4 ml) and concentrated to give 4-[(1,1-dimethylpropyl)amino]-3,5,6-trifluoro-1,2-benzenedicarboxylic acid, dimethyl ester as an oil. Hydrochloric acid (36% aqueous solution), 20 ml, is added to this oil and the resulting mixture is heated at reflux for 20 hours. The solution is concentrated to 4-5 ml and then diluted with water (20 ml). Cooling gave crystals which are collected and vacuum dried to give 1.2 g of 3-amino-2,4,5-trifluorobenzoic acid (63%); mp 133° -136° C.; GC (97.9%); HPLC (94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04885386 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-fb642c51183e405c8b98af896c6a7963 |
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| Source note | uspto-grants-1989_12 |
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