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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106631Generated: November 1, 2026

3,4-Dichlorobenzaldehyde → HCID 18789260, compound

https://huagongshe.com/reaction/1106631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichlorobenzaldehydeHCID 22710—
Reactant2-(4-Methoxybenzyl)isothioureaHCID 415139—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetateHCID 22005512—
SolventDimethylformamideHCID 6228—
ProductHCID 18789260HCID 1878926025.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 3-phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate (1.0 g, 2.88 mmol), 3,4-dichlorobenzaldehyde (0.60 g, 3.45 mmol), 2-(4-methoxybenzyl)isothiourea (0.80 g, 3.45 mmol) and sodium hydrogen carbonate (0.29 g, 3.45 mmol) was stirred in N,N-dimethylformamide (10 mL) for 6 days at room temperature, then heated to 50° C. for 7 days. The DMF was removed in vacuo and ethyl acetate was added to the residue. The precipitate was removed by filtration and the filtrate was washed with water, sodium hydrogen carbonate solution and brine, dried and evaporated to yield an oil. This oil was further purified by flash chromatography to give the title compound (0.50 g) as an oil. The oil can be converted into a mono or dihydrochloride salt, by dissolution in ether and addition of one or two equivalents of hydrogen chloride. Electrospray MSm /z 682/684 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057332
Source datasetuspto-grants-2000_05
ORD IDord-26a4fb1d35d143e7bbcf9a7b84c018b3
Source noteuspto-grants-2000_05