HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106631Generated: November 1, 2026
3,4-Dichlorobenzaldehyde → HCID 18789260, compound
https://huagongshe.com/reaction/1106631
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dichlorobenzaldehyde | HCID 22710 | — |
| Reactant | 2-(4-Methoxybenzyl)isothiourea | HCID 415139 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate | HCID 22005512 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18789260 | HCID 18789260 | 25.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057332 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-26a4fb1d35d143e7bbcf9a7b84c018b3 |
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| Source note | uspto-grants-2000_05 |
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