HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106630Generated: October 31, 2026
3,4-Dichlorobenzaldehyde → HCID 9851145, compound
https://huagongshe.com/reaction/1106630
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dichlorobenzaldehyde | HCID 22710 | — |
| Reactant | 2-Methyl-2-thiopseudourea sulfate | HCID 75270 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate | HCID 22005512 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 9851145 | HCID 9851145 | 10.2% |
Reaction Steps
A mixture of 3-phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate (10.6 g, 30.6 mmol), 3,4-dichlorobenzaldehyde (5.9 g, 34.0 mmol), 2-methyl-2-thiopseudourea sulfate (6.15 g, 22.1 mmol) and sodium acetate (2.78 g, 34.0 mmol) was stirred in N,N-dimethylformamide (50 mL) for 4 days at room temperature, then heated to 60° C. for 24 h. 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 (1.3 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 576/578 [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-8b7a925018cd4d06a61c672972a64284 |
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| Source note | uspto-grants-2000_05 |
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