HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072827Generated: October 27, 2026
Iodine → 3,3'-Difluoro-4,4'-dihydroxybiphenyl
https://huagongshe.com/reaction/2072827
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | 4-Bromo-2-fluoroanisole | HCID 75378 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178491915 | HCID 178491915 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,3'-Difluoro-4,4'-dihydroxybiphenyl | HCID 520956 | — |
Reaction Steps
Flaky metallic magnesium (2.43 g) was added to 50 ml of dry tetrahydrofuran, and while the mixture was heated, a solution of 20.5 g of 4-bromo-2-fluoroanisole in 100 ml of dry tetrahydrofuran was added dropwise little by little in a stream of nitrogen to prepare a tetrahydrofuran solution of 3-fluoro-4-methoxy-phenyl magnesium bromide. Then, 18.0 g of 4-bromo-2-fluoroanisole was added to 100 ml of dry tetrahydrofuran containing 0.05 g of iodine and 0.1 g of palladium chloride. The mixture was maintained at 40° to 50° C. in a stream of nitrogen, and the above-prepared tetrahydrofuran solution of 3-fluoro-4-methoxyphenyl magnesium bromide was added dropwise gradually. The addition was completely in about 1 hour, and thereafter, the mixture was reacted for 5 hours at the refluxing temperature of tetrahydrofuran. After the reaction, the reaction mixture was after-treated in a customary manner to give 38.2 g of a crude product. The desired product was isolated from the crude product by silica gel column chromatography using ethyl acetate/hexane as an eluent. Thus, 15.0 g of 3,3'-difluoro-4,4'-dimethoxybiphenyl was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04914224 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-a655054f75c74ba7bf99e19e5fbf24bd |
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| Source note | uspto-grants-1990_04 |
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