HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127911Generated: November 2, 2026
2,2,2-Trifluoroethanol → HCID 12906276, compound
https://huagongshe.com/reaction/127911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 12906275 | HCID 12906275 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12906276 | HCID 12906276 | — |
Reaction Steps
To a stirred mixture of 470 g (1.42 mole) of 2,3,7-trichloro-6-quinoxalinesulfonyl chloride and 153 g (1.53 mole) of 2,2,2-trifluoroethanol in 3 liters of anhydrous tetrahydrofuran are added 183 g (1.42 mole) of N,N-diisopropylethylamine. The resulting mixture is heated under reflux with exclusion of moisture for 24 hours. The solvent is removed under reduced pressure to obtain a residue which is dispersed in one liter of diethyl ether. The resulting mixture is washed twice with 500 ml of water then dried over magnesium sulfate, and filtered. The filtrate obtained therefrom is evaporated to give crude product which is recrystallized first from cyclohexane and then from 2-propanol to give 112 g (20%) of nearly colorless crystals having a melting point of 142°-144°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04258044 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-e7efe5bf9ad64393998762b0a3167b43 |
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| Source note | uspto-grants-1981_03 |
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