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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833182Generated: October 31, 2026

Ethyl Acetate → HCID 22048326, compound

https://huagongshe.com/reaction/1833182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 86595640HCID 86595640—
SolventMethanolHCID 887—
ProductHCID 22048326HCID 22048326109.2%

Reaction Steps

To a solution of 6-(3-acetoxy-propoxy)-1-(3-ethoxy-benzyl)-4-formyl-7-methoxy-1H-isoquinoline-2-carboxylic acid ethyl ester (130 mg, 0.25 mmol) in methanol (3.5 mL) was added powdered potassium hydroxide (85.5 mg, 1.53 mmol) at room temperature. The mixture was stirred at room temperature for 14 hrs. The solvent was evaporated and the residue was diluted with water (20 mL). The aqueous phase was extracted with ethyl acetate (2×20 mL). The combined extracts were washed with saturated aqueous sodium chloride solution (20 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to afford a crude oil. Flash chromatography (Merck Silica gel 60, 70–230 mesh, 50% ethyl acetate/hexane, 75% ethyl acetate/hexane, ethyl acetate) afforded 6-(3-acetoxy-propoxy)-7-methoxy-1-(3-ethoxy-benzyl)-1,2-dihydro-isoquinoline-4-carbaldehyde (120 mg, 42% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067529B2
Source datasetuspto-grants-2006_06
ORD IDord-6fb7dbeb44494be39e4524d8eb9a671c
Source noteuspto-grants-2006_06