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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947192Generated: November 1, 2026

Oxalyl chloride → HCID 59829891, compound

https://huagongshe.com/reaction/1947192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantBenzenamine, 4-(4-morpholinyl)-HCID 75655—
ReactantSodium BicarbonateHCID 516892—
Reactant2,4-Dibenzyloxy-5-isopropyl-benzoic acidHCID 59167879—
CatalystDimethylformamideHCID 6228—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59829891HCID 5982989187%

Reaction Steps

A dichloromethane (30 mL) solution of 2,4-bis-benzyloxy-5-isopropylbenzoic acid (F370-IM1, 2 g, 5.31 mmol) was mixed with dimethylformamide (0.053 mL, 0.05 mmol) and oxalylchloride (0.61 mL, 6.38 mmol) under ice cold conditions and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue thus obtained was dissolved in tetrahydrofuran (30 mL) and pyridine (10 mL). To the solution was added 4-(4-morpholino)aniline (1.04 g, 5.84 mmol) under ice cold conditions. The reaction was carried out at room temperature for 1 hour. Dichloromethane (50 mL) and 5% aqueous sodium hydrogencarbonate (20 mL) were added to the reaction mixture. The aqueous layer was separated and extracted with dichloromethane, the combined organic layers thus obtained were washed with saturated aqueous sodium chloride solution (30 mL) and dried over anhydrous sodium sulfate. Sodium sulfate was removed by filtration, and the solvent was distilled off under reduced pressure. To the residue were added ethyl acetate (5 mL), toluene (5 mL) and hexane (20 mL), and the resulting suspension was stirred at room temperature for 1 hour. The precipitated solid was collected by filtration to obtain the title compound (F370-IM2: white crystals, 2.47 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399464B2
Source datasetuspto-grants-2013_03
ORD IDord-e5e141f929bc46d8afa2f261dc73563c
Source noteuspto-grants-2013_03