HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221872Generated: October 30, 2026
2-Methoxyethylamine → 3-Bromo-n-(2-methoxyethyl)benzenesulfonamide
https://huagongshe.com/reaction/221872
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | m-Bromobenzenesulphonyl chloride | HCID 17943 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Bromo-n-(2-methoxyethyl)benzenesulfonamide | HCID 47108460 | 96% |
Reaction Steps
To a solution of 3-bromobenzenesulfonyl chloride (1.00 g, 3.72 mmol) in acetone (10 mL) was added 2-methoxyethylamine (0.97 mL, 11.15 mmol, 3.0 eq) and potassium carbonate (2.57 g, 18.6 mmol, 5.0 eq), and the reaction was stirred at 40° C. for 5 h. The mixture was cooled to room temperature and then partitioned between EtOAc and water, and the organic phase was washed with brine, dried over MgSO4, and concentrated at reduced pressure. The residue was purified by MPLC (20% to 25% EtOAc/hexane) to give 1.05 g (96%) of the desired product as an oil. TLC [30% EtOAc/hexane], Rf=0.33.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207166B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-c96d4e9e91e44908a7bf78c940c12a25 |
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| Source note | uspto-grants-2012_06 |
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