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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440839Generated: October 29, 2026

Water → 3-Dipropylamino-5-acetylchroman

https://huagongshe.com/reaction/1440839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Dipropylamino-5-chloroformyichromanHCID 19028084—
Reactant3-Dipropylamino-5-methyloxycarbonylchromanHCID 19028093—
ReactantHCID 178418348HCID 178418348—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
Product3-Dipropylamino-5-acetylchromanHCID 10221213—

Reaction Conditions

Temperature-78 °C

Reaction Steps

3-Dipropylamino-5-chloroformylchroman*HCl (4.42 g, 13.4 mmol), prepared from 3-dipropylamino-5-methyloxycarbonylchroman (Example 2) analogous to the procedure used in Example 3, in dry tetrahydrofuran (20 ml), was added to a pre-formed solution of lithium dimethylcuprate; prepared from MeLi and CuI, in 200 mL tetrahydrofuran at -78° C. The solution was stirred for 15 minutes at -78° C. and was then allowed to reach room temperature during 10 minutes. Then, 30 mL H2O was slowly added. The organic phase was decanted, dried with Na2SO4 and evaporated to dryness. The residue was purified by flash chromatography (silica gel) by elution with ethyl acetate/hexane 1:8. The title compound was crystallized as salt from ethyl acetate. Mp 106°-108° C. (oxalate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05500425
Source datasetuspto-grants-1996_03
ORD IDord-dac425d4dd7d440aa4d24c8506b7c6e3
Source noteuspto-grants-1996_03