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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73163Generated: October 25, 2026

Triphenylphosphine → 3-[Isopropyl-(4-oxo-cyclohexanecarbonyl)-amino]-5-phenyl-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/73163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Oxocyclohexanecarboxylic acidHCID 192730—
ReactantMethyl 3-(isopropyl-amino)-5-phenylthiophene-2-carboxylateHCID 11737447—
ReactantN-chlorosuccinamideHCID 15238416—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product3-[Isopropyl-(4-oxo-cyclohexanecarbonyl)-amino]-5-phenyl-thiophene-2-carboxylic acid methyl esterHCID 59752367—

Reaction Steps

To a solution of 3-Isopropylamino-5-phenyl-thiophene-2-carboxylic acid methyl ester (1.5 g, 5.45 mmol) in 1,2-dichloroethane, N-chlorosuccinamide (0.940 g, 7.091 mmol), triphenylphosphine (1.9 g, 7.091 mmol) and 4-oxo-cyclohexanecarboxylic acid (800 mg, 5.455 mmol) were added. The reaction mixture was stirred at reflux for overnight under an atmosphere of N2. The reaction mixture was diluted with CH2Cl2 and extracted with saturated solution oh NaHCO3. The organic layer was separated, dried (Na2SO4) and concentrated. The residue was purified using silica gel column chromatography using ethyl acetate:hexane (1:4) as eluent to obtain 3-[Isopropyl-(4-oxo-cyclohexanecarbonyl)-amino]-5-phenyl-thiophene-2-carboxylic acid methyl ester. (1.2 g, 55%) as syrup. 1H NMR (CDCl3, 400 MHz): δ7.75-7.50 (m, 2H), 7.70-7.38 (m, 3H), 7.12 (s, 1H), 4.95 (m, 1H), 3.87 (s, 3H), 2.75-0.83 (m, 15H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829030B2
Source datasetuspto-grants-2014_09
ORD IDord-f136c2155e5048dbbc5cd26ffa9647f9
Source noteuspto-grants-2014_09