HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40967Generated: October 28, 2026
Water → 1-Bromo-3-(ethanesulfonyl)benzene
https://huagongshe.com/reaction/40967
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 1-Bromo-3-(ethylsulfanyl)benzene | HCID 13082727 | — |
| Product | 1-Bromo-3-(ethanesulfonyl)benzene | HCID 57477908 | 92% |
Reaction Steps
The MCPBA (2.37 g, 10.6 mmol) was added to a solution of 1-bromo-3-(ethylthio)benzene (1.00 g, 4.80 mmol) in DCM (10 ml, 156 mmol) cooled to 0° C. The reaction was stirred for 1 h and then was diluted with water and extracted with ethyl acetate three times. The combined organic layers were dried with magnesium sulfate, filtered, and concentrated in vacuo. The resulting crude residue was purified by flash column chromatography with a hexane:ethyl acetate gradient to give 1-bromo-3-(ethylsulfonyl)benzene as a colorless oil 1.1 gm 92%, 1H NMR (300 MHz, CDCl3): δ□8.09(m, 1H), 7.85(d,1H), 7.78(d, 1H) 7.45(t,1H), 3.14(q, 2H), 1.25(t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530485B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-dec1a45742ad401eab44df908c4ab231 |
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| Source note | uspto-grants-2013_09 |
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