HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447834Generated: October 30, 2026
Triphenylphosphine → 4-(Bromomethyl)-1-fluoro-2-(methylsulfonyl)benzene
https://huagongshe.com/reaction/447834
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Fluoro-3-(methylsulfonyl)benzenemethanol | HCID 66877838 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(Bromomethyl)-1-fluoro-2-(methylsulfonyl)benzene | HCID 66877626 | — |
Reaction Steps
(Step 1) Triphenylphosphine (3.21 g) was suspended in acetonitrile (50 ml), bromine (0.64 ml) was added, and the mixture was stirred for 30 min. [4-Fluoro-3-(methylsulfonyl)phenyl]methanol (2.5 g) was added to the reaction mixture, and the mixture was stirred at 85° C. for 20 hr, treated with aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by basic silica gel chromatography (ethyl acetate:hexane=1:1) to give 4-(bromomethyl)-1-fluoro-2-(methylsulfonyl)benzene (1.64 g). 1H NMR (300 MHz, CDCl3) 8 ppm 3.24 (3H, s), 4.49 (2H, s), 7.19-7.31 (1H, m), 7.62-7.74 (1H, m), 7.99 (1H, dd, J=6.50, 2.35 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481569B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-9d8465140fa548818ea2faaeb4f0fb2d |
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| Source note | uspto-grants-2013_07 |
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