HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363100Generated: November 1, 2026
Potassium Carbonate → 4-(2-Chlorobenzyloxy)-3,5-dichlorophenoxyacetaldehyde diethyl acetal
https://huagongshe.com/reaction/363100
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | 4-(2-Chlorobenzyloxy)-3,5-dichlorophenol | HCID 54095899 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-Chlorobenzyloxy)-3,5-dichlorophenoxyacetaldehyde diethyl acetal | HCID 54075232 | 72% |
Reaction Steps
A mixture of 0.85 g of 4-(2-chlorobenzyloxy)-3,5-dichlorophenol, 0.47 ml of bromoacetaldehyde diethyl acetal, 0.46 g of potassium carbonate and 20 ml of N,N-dimethylformamide was stirred at 90° C. for 6 hours. After cooling to room temperature, the reaction mixture was poured into ice water, and extracted twice with 50 ml of diethyl ether. The combined ether layer was washed with water, and dried with anhydrous magnesium sulfate, followed by removal of the solvent by distillation under reduced pressure. The residue was subjected to silica gel chromatography, which afforded 0.85 g of 4-(2-chlorobenzyloxy)-3,5-dichlorophenoxyacetaldehyde diethyl acetal (72% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05872137 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-6300e521e43f44889713381f2ba869df |
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| Source note | uspto-grants-1999_02 |
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