HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703435Generated: October 30, 2026
Benzene, 1-chloro-4-fluoro- → 4-Chlorophenyl phenyl ether
https://huagongshe.com/reaction/1703435
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene, 1-chloro-4-fluoro- | HCID 9604 | — |
| Reactant | Potassium phenoxide | HCID 23670670 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 4-Chlorophenyl phenyl ether | HCID 23436 | 54.2% |
Reaction Steps
A stirred solution containing 14.8 g (0.112 mole) of potassium phenoxide and 13.1 g (0.10 mole) of p-fluorochlorobenzene in 100 ml of N-methyl-2-pyrrolidinone is heated at reflux for a period of time necessary to effect complete reaction, as determined by vapor phase chromotography techniques. The crude reaction mixture is cooled and diluted to a volume of 400 ml with water, whereupon it is extracted with several portions of ether. The combined organic extracts are washed with a 5% sodium hydroxide solution, water, and a saturated sodium chloride solution, dried (magnesium sulfate), and concentrated in vacuo. Distillation at reduced pressure affords 11.1 g (54%) of material, b(0.05 mm) 73.5°-75.5°, whose spectral properties are in agreement with the desired structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04124370 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-b3412459b0ec4907a094e0e03353d75c |
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| Source note | uspto-grants-1978_11 |
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