HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360593Generated: October 30, 2026
Phenethyl bromide → 4-(2-Bromoethyl)benzenesulfonyl chloride
https://huagongshe.com/reaction/2360593
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(2-Bromoethyl)benzenesulfonyl chloride | HCID 12846775 | 80.6% |
Reaction Steps
To a solution of 2-bromoethylbenzene (10.0 g; 54 mmol) in 16 ml of chloroform placed at a temperature of 0° C. was added dropwise a solution of chlorosulfonic acid (162 mmol, 18.87 g; 10.82 ml) in 11 ml of chloroform. After 15 minutes at 0° C., the reaction was maintained at room temperature for 3 hours. The reaction mixture was poured onto ice, and the aqueous phase was extracted with chloroform. The combined organic phases were washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was evaporated off to give 12.34 g of crude product, which was purified by chromatography on a column of silica, eluting with chloroform (76% yield). The product obtained was used for the following reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686147B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-32f1c94e187f430c8540b35bf68c0823 |
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| Source note | uspto-grants-2014_04 |
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