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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015664Generated: October 30, 2026

1,4-Dioxane → HCID 16074922, compound

https://huagongshe.com/reaction/1015664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantCyclopropanecarbonyl chlorideHCID 77637—
ReactantHCID 23677633HCID 23677633—
SolventWaterHCID 962—
ProductHCID 16074922HCID 1607492231.5%

Reaction Steps

To a solution of sodium 3-benzylamino-5-phenyl-thiophene-2-carboxylate (41.1 mg, 0.1 mmol) was added 32 mg (0.3 mmol) of cyclopropanecarbonyl chloride, 1.5 ml of dioxane and 0.5 ml of water. The mixture was stirred overnight at room temperature and concentrated in vacuo. A 4N hydrogen chloride solution in dioxane (1 ml) was added and the mixture was stirred for one hour at room temperature. The mixture was again concentrated and the crude material was purified by reverse phase HPLC giving access to 11.9 mg (31.5%) of 3-(benzyl-cyclopropanecarbonyl-amino)-5-phenyl-thiophene-2-carboxylic acid as a pale yellow solid. NMR 1H (DMSO D6, 400 MHz): 7.56-7.54 ppm (m, 2H, Haro); 7.39-7.13 ppm (m, 10H, Haro, Hazole and COOH); 5.27 ppm (d, 1H, J=15.2 Hz); 4.48 ppm (d, 1H, J=15.2 Hz); 1.49 ppm (m, 1H); 0.77 ppm (m, 2H); 0.61 ppm (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985769B2
Source datasetuspto-grants-2011_07
ORD IDord-8d92341cff4c426a8222630fc28a7f52
Source noteuspto-grants-2011_07