HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582702Generated: October 31, 2026
Dimethylcarbamoyl Chloride → HCID 11198140, compound
https://huagongshe.com/reaction/1582702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178505882 | HCID 178505882 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11198140 | HCID 11198140 | 47.1% |
Reaction Steps
A solution of 3-[4-(4-fluorophenoxy)phenyl]-1H-pyrazole (467 mg, 1.84 mmol) in 7 mL of THF containing 0.3 mL (2.13 mmol) of triethylamine was treated with 0.3 mL (3.2 mmol) dimethylcarbamyl chloride added via syringe. No reaction was observed at room temperature. An additional 0.3 mL of dimethylcarbamyl chloride was added and the reaction was heated at reflux overnight. The reaction was then added to a saturated aqueous NaHCO3 solution and EtOAc. The aqueous layer was washed with EtOAc and the pooled organic layers were dried (Na2SO4), filtered and concentrated to dryness. Column chromatography (7/3 hexane/EtOAc) afforded 282 mg of the title compound as a yellow oil that solidified on standing, mp 59-63° C. 1H NMR (CDCl3): δ 8.15 (d, 1H, J=2.7 Hz), 7.80 (d, 2H, J=8.4 Hz), 7.06-6.88 (m, 6H), 6.62 (d, 1H, J=2.7 Hz), 3.30 (br s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06737418B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-05a44f8ebe0444bab5e032428bd92818 |
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| Source note | uspto-grants-2004_05 |
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