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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820010Generated: November 1, 2026

Hydrochloric Acid → HCID 23090950, compound

https://huagongshe.com/reaction/1820010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantHCID 23090958HCID 23090958—
ReactantHCID 178418255HCID 178418255—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 23090950HCID 23090950—

Reaction Steps

To a solution of phenylmagnesium bromide (2 mol/l THF solution, 1.6 ml) in toluene (7 ml) was added dropwise a solution of N-methoxy-N-methyl-4-{4-[1-(1-pyrrolidinyl)ethyl]phenyl}butanamide (200 mg, 0.66 mmol) obtained in Reference Example 89 in toluene (3 ml) under a nitrogen atmosphere under ice-cooling. After stirring at room temperature for 1 hr, the reaction solution was poured into water (40 ml), and extracted with ethyl acetate (40 ml×2). The extract was washed successively with 10% sodium hydrogencarbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by NH-silica gel column chromatography (developing solvent; hexane:ethyl acetate=10:1) to give a colorless oil. The oil was dissolved in ethyl acetate (10 ml), and 4N-hydrochloric acid (ethyl acetate solution; 0.2 ml) was added dropwise under ice-cooling. The mixture was stirred for 5 min., and the solvent was evaporated under reduced pressure. The residue was powderized with isopropyl ether and hexane, and washed with hexane to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601868B2
Source datasetuspto-grants-2009_10
ORD IDord-e5b71e6ac2294ce7b12bf7baf55c2862
Source noteuspto-grants-2009_10