HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485771Generated: October 30, 2026
3,4-Dihydroxybenzaldehyde → 3,4-Bis[(3,4-dichlorophenyl)methoxy]benzaldehyde
https://huagongshe.com/reaction/485771
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Bromomethyl)-1,2-dichlorobenzene | HCID 639726 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3,4-Bis[(3,4-dichlorophenyl)methoxy]benzaldehyde | HCID 20247936 | 84.1% |
Reaction Steps
To a solution of 2 g of 3,4-dihydroxybenzaldehyde in 40 ml of acetone, were added 4.40 g of anhydrous potassium carbonate and 6.24 g of 3,4-dichlorobenzyl bromide. The mixture was refluxed for 24 hours. The reaction mixture was then removed of the acetone by distillation under reduced pressure, admixed with 200 ml of water, and the intended product was extracted with 200 ml of chloroform. The chloroform layer was dried over anhydrous sodium sulfate, and stripped of the chloroform by distillation under reduced pressure to precipitate white crystals. The raw crystals were recrystallized from ethyl alcohol to give 4.99 g of colorless crystals having a melting point of 181°-183° C. The IR absorption spectrum of the compound, as measured in KBr-tablet, showed the following absorption maxima (in wave number, cm-1) 658, 693, 710, 760, 795, 805, 830, 875, 1030, 1135, 1168, 1200, 1245, 1280, 1370, 1403, 1437, 1460, 1470, 1510, 1585, 1600, 1690, 2730, 2830, 2870, 2910, and 3070.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04537880 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-ead68e3688074f0d9b967b9bccc884a3 |
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| Source note | uspto-grants-1985_08 |
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