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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638804Generated: October 31, 2026

Ethyl Acetate → HCID 13428535, compound

https://huagongshe.com/reaction/1638804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(Chloromethyl)-1,2,3-trimethoxybenzeneHCID 77448—
Reactant1,4-diazepane-1-carbaldehydeHCID 7006656—
SolventWaterHCID 962—
ProductHCID 13428535HCID 1342853531.5%

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 3,4,5-trimethoxybenzyl chloride (10.5 g), N-formyl homopiperazine (6.82 g), potassium carbonate (8 g) and ethyl acetate (40 ml) is heated at 50-60° C. for 4 hours. After addition of water the reaction mixture is shaken thoroughly. The organic layer is separated, washed with water, dried and evaporated under reduced pressure. To the residue is added 10% hydrochloric acid (20 ml), and the mixture is extracted with ethyl acetate. The aqueous layer is made alkaline (>pH 9) with a 20% aqueous solution of sodium hydroxide, and extracted with methylene chloride. The extract solution is evaporated under reduced pressure. To the residue is added 10% hydrochloric acid (15 ml), and the mixture is stirred at 100° C. for 3 hours. The reaction mixture is made alkaline with a 20% aqueous solution of sodium hydroxide, and extracted with ethyl acetate. The extract solution is dried and evaporated under reduced pressure. The residue is converted to the hydrochloride in a mixture of ethyl acetate and ethanol to yield 1-(3,4,5-trimethoxybenzyl) homopiperazine dihydrochloride (2.7 g) as colorless powdery crystals, m.p. 216°-220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880809
Source datasetuspto-grants-1989_11
ORD IDord-4ae78cdc6be4411cb8e1dd65d8c0dafe
Source noteuspto-grants-1989_11