HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851289Generated: October 30, 2026
Phenolate Sodium → 3-Phenoxy-4-fluoro-benzaldehyde dimethyl acetal
https://huagongshe.com/reaction/851289
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenolate Sodium | HCID 4445035 | — |
| Reactant | 2-Bromo-4-(dimethoxymethyl)-1-fluorobenzene | HCID 22260864 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | 3-Phenoxy-4-fluoro-benzaldehyde dimethyl acetal | HCID 20502042 | 75.4% |
Reaction Steps
0.4 g of copper-I bromide and 43.5 g (0.375 mole) of sodium phenolate were added to 95 ml of diethylene glycol dimethyl ether (diglyme). The temperature of the mixture rose to about 80° C. To effect dehydration, 15 ml of diglyme (boiling point 160° C.) were distilled off under normal pressure. 57.3 g (0.23 mole) of 3-bromo-4-fluoro-benzaldehyde dimethyl acetal were then added dropwise in the course of 10 minutes, at 150°-155° C., and the reaction mixture was stirred for a further 7 hours at 155° C. Gas chromatography indicated that all of the precursor had then been converted. Subsequently, the solvent was distilled off at 40° C./10 mm Hg, the residue was dissolved in 300 ml of toluene and, after adding 10 g of "Celite" (Trade Mark) 545 as a filter aid, the mixture was filtered to remove the inorganic material. The filtrate was washed with twice 100 ml of 50% strength sodium hydroxide solution, the solvent was then stripped off in vacuo and the residue was distilled in vacuo. 45.5 g (75. of theory) of 3-phenoxy-4-fluoro-benzaldehyde dimethyl acetal were thus obtained in the form of a colorless oil with a boiling point of 128°-130° C./0.1 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04383949 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-505159c447234f3ab842ecc7e8fe5c33 |
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| Source note | uspto-grants-1983_05 |
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