HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072272Generated: October 27, 2026
Water → 2,3,5,6-Tetrafluorobenzenedimethanol
https://huagongshe.com/reaction/1072272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 2,3,5,6-Tetrafluoroxylylenediamine | HCID 68863371 | — |
| Product | 2,3,5,6-Tetrafluorobenzenedimethanol | HCID 66712953 | 74.5% |
Reaction Steps
Into a 200 ml-volume flask equipped with a thermometer, a stirring unit, a nitrogen inlet and a reflux condenser, 10.4 g (50.0 mmol) of 2,3,5,6-tetrafluoroxylylenediamine synthesized in Example 1, 50 g of water and 10.35 g (150.0 mmol) of sodium nitrite were charged, and the mixture was stirred at room temperature for 30 minutes. Subsequently, under cooling of the reactor in a water bath, 6.13 g (62.5 mmol) of sulfuric acid was added dropwise over 60 minutes while keeping the inside of the reaction system at 40° C. or less. The reaction solution obtained was extracted with 10.0 g of methyl ethyl ketone, the organic phase was washed with 5.0 g of an aqueous 5 mass % sulfuric acid solution, and then the methyl ethyl ketone was removed by distillation, as a result, 7.9 g of 2,3,5,6-tetrafluorobenzenedimethanol was obtained as white crystals. The purity determined from the GC area in percentage was 98.3% and the yield was 73.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06909023B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-02e72b8f9eed45aab240839a38b5d509 |
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| Source note | uspto-grants-2005_06 |
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