HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708567Generated: October 30, 2026
Potassium Carbonate → 3-(2-(4-((3,4-Dichlorobenzyl)oxy)phenyl)-2-oxoethoxy)-4-fluorobenzonitrile
https://huagongshe.com/reaction/708567
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluoro-3-hydroxybenzonitrile | HCID 20776981 | — |
| Reactant | 2-Bromo-1-[4-(3,4-dichloro-benzyloxy)-phenyl]-ethanone | HCID 58327574 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-(2-(4-((3,4-Dichlorobenzyl)oxy)phenyl)-2-oxoethoxy)-4-fluorobenzonitrile | HCID 58327162 | 102% |
Reaction Steps
4-Fluoro-3-hydroxy-benzonitrile (15 g), 2-bromo-1-[4-(3,4-dichloro-benzyloxy)-phenyl]-ethanone (45 g), and potassium carbonate 45 g) were suspended together in 630 mL acetone with stirring. The mixture continued to stir for 18 hours, then was concentrated to dryness. The solid residue was taken up in 500 mL diethyl ether and stirred 1.5 h, then 1 L water was added and stirred vigorously an additional 3 hours. The solid product was collected by filtration and washed with 200 mL diethyl ether three times. It was then dissolved in THF, filtered to remove any remaining inorganic salt, and evaporated again to dryness. After drying under vacuum 18 h, 48 g of desired product was obtained (quantitative). 1H NMR (400 MHz, DMSO-d6): 7.97 (d, 2H), 7.66 (d, 1H), 7.45 (m, 2H), 7.46 (m, 3H), 7.16 (d, 2H), 5.72 (s, 2H), 5.25 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09175003B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-b20fcf7748924b098ed0d5560ef4fae4 |
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| Source note | uspto-grants-2015_11 |
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