HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339836Generated: October 26, 2026
Water → 1-(3-Bromophenyl)-2-hydroxy-2-methylpropane-1-sulfonamide
https://huagongshe.com/reaction/339836
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(2,4-Dimethoxybenzyl)-1-(3-bromophenyl)-2-hydroxy-2-methylpropane-1-sulfonamide | HCID 68291617 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3-Bromophenyl)-2-hydroxy-2-methylpropane-1-sulfonamide | HCID 68291860 | 70.8% |
Reaction Steps
A solution of 8.63 g of N-[2,4-dimethoxybenzyl]-1-(3-bromophenyl)-2-hydroxy-2-methylpropane-1-sulfonamide in 40 ml of dichloromethane was admixed with 10 ml of trifluoroacetic acid and stirred at room temperature for 30 minutes. The reaction solution was admixed with 40 ml of water, and gradually and cautiously with 150 ml of a saturated aqueous sodium hydrogencarbonate solution. The precipitate was filtered off with suction, washed with water and dried over P2O5 under reduced pressure. The crude product was purified by means of normal phase chromatography using a Flashmaster with a dichloromethane/methanol gradient. The product-containing fractions were combined and concentrated by rotary evaporation. This gave the product (4.11 g) with a molecular weight of 308.2 g/mol (C10H14BrNO3S); MS (ESI): m/e=325 (M+H2O+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895547B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-905a95438271452d9c55378432525c8a |
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| Source note | uspto-grants-2014_11 |
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