HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015697Generated: October 30, 2026
Water → 2-(Bromomethyl)-4-chloro-1-(methylsulfonyl)benzene
https://huagongshe.com/reaction/1015697
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | (5-Chloro-2-(methylsulfonyl)phenyl)methanol | HCID 66885987 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(Bromomethyl)-4-chloro-1-(methylsulfonyl)benzene | HCID 66877551 | — |
Reaction Steps
(Step 3) Triphenylphosphine (1.19 g) was suspended in acetonitrile (50 ml), bromine (0.24 ml) was added, and the mixture was stirred at room temperature for 30 min. A solution of [5-chloro-2-(methylsulfonyl)phenyl]methanol obtained in Step 2 (1 g) in acetonitrile (10 ml) was added to the reaction mixture. The mixture was stirred at 70° C. for 3 hr, treated with water, and extracted with ethyl acetate. The extract was washed successively with aqueous sodium hydrogen carbonate solution and 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=1:3) to give 2-(bromomethyl)-4-chloro-1-(methylsulfonyl)benzene (0.46 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985862B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-809d4a8387f142ac9fae5a32e12cf581 |
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| Source note | uspto-grants-2011_07 |
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