HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729252Generated: October 31, 2026
Hydrochloric Acid → HCID 68661688, compound
https://huagongshe.com/reaction/729252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | N-ethyl-1-[4-(trifluoromethyl)phenyl]methanesulfonamide | HCID 68662627 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68661688 | HCID 68661688 | 81.6% |
Reaction Steps
Potassium tert-butoxide (0.309 g, 1.83 mmol) was added to a solution of N-ethyl-1-[4-(trifluoromethyl)phenyl]methanesulfonamide (0.49 g, 1.83 mmol) and diethyl oxalate (0.322 g, 2.20 mmol) in THF (4 mL) at 0° C. The mixture was heated in a microwave reactor at 150° C. for 10 mins. HCl (1M, 2 mL) was added dropwise to the mixture at 0° C. It was evaporated and the residue was extracted with DCM. The organic layer was dried and evaporated to give the title compound (0.480 g, 81%) as a solid; 1H NMR (500 MHz, CDCl3): δ 8.05 (d, 2H), 7.77 (d, 2H), 3.87 (q, 2H), 1.49 (t, 3H); Mass Spectrum: M−H+ 320.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582629B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-8cda38af14924b15933ff6035202f0db |
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| Source note | uspto-grants-2009_09 |
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