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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882713Generated: October 28, 2026

Hydrochloric Acid → HCID 23169890, compound

https://huagongshe.com/reaction/882713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-(4-Methoxyphenyl)cyclopropane-1-carboxylic acidHCID 85575—
ReactantAluminium lithium hydrideHCID 21226445—
CatalystHCID 178419074HCID 178419074—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23169890HCID 2316989084%

Reaction Steps

Under an argon atmosphere, a solution of 1-(4-methoxyphenyl)cyclopropane carboxylic acid (2.00 g, 10.4 mmol) in tetrahydrofuran (20 mL) was added with lithium aluminum hydride (513 mg, 13.5 mmol) at 0° C., and the resultant was stirred at room temperature for 2 hours. The resultant was added sequentially with water and hydrochloric acid at 0° C., stirred at room temperature for 30 min and then extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and concentrated in vacuo. The obtained residue was dissolved in dichloromethane (15 mL). The resultant was sequentially added with molecular sieves 4β (1.80 g), N-methylmorpholine (1.83 g, 15.6 mmol) and tetrapropylammonium perruthenate (1.83 mg, 0.520 mmol) at 0° C., and stirred at room temperature for 1.5 hours. The reaction solution was filtered using celite, and concentrated in vacuo. The obtained residue was purified using column chromatography (hexane:ethyl acetate=4:1), and 1-(4-methoxyphenyl)cyclopropane carboaldehyde (1.54 g, 84.0%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236789B2
Source datasetuspto-grants-2012_08
ORD IDord-4a07631c94d94d14a87270c501eedc31
Source noteuspto-grants-2012_08