HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243850Generated: October 30, 2026
1-Bromo-4-fluorobenzene → HCID 21929393, compound
https://huagongshe.com/reaction/1243850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl methoxyacetate | HCID 80507 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21929393 | HCID 21929393 | — |
Reaction Steps
4.9 g of magnesium, 5 cm3 of 4-bromofluorobenzene and 25 cm3 of tetrahydrofuran are heated to a temperature in the region of 60° C. 17 cm3 of 4-bromofluorobenzene in solution in 25 cm3 of tetrahydrofuran are added and the mixture is heated at a temperature in the region of 60° C. for 2 hours. 5 cm3 of methyl methoxyacetate in solution in 25 cm3 of tetrahydrofuran are added to the solution prepared above, cooled to a temperature in the region of 0° C. After stirring for 24 hours at a temperature in the region of 20° C., the reaction mixture is poured into 200 cm3 of saturated aqueous ammonium chloride solution and extracted with three times 75 cm3 of ethyl acetate, and the organic phases are washed with twice 100 cm3 of distilled water, dried over magnesium sulphate and concentrated to dryness under reduced pressure. The residue obtained is purified by flash chromatography on silica gel (35–70 μm), eluting with pure dichloromethane; 9.8 g of 1,1-bis(4-fluorophenyl)-2-methoxyethanol are thus obtained in the form of a yellow oil, the characteristics of which are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119115B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-3c9ee98719d44da2a5e2ad737730080f |
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| Source note | uspto-grants-2006_10 |
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