HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421555Generated: November 1, 2026
Hydrochloric Acid → HCID 86629171, compound
https://huagongshe.com/reaction/421555
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(3,4-dimethoxyphenyl)benzenesulfonamide | HCID 808173 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86629171 | HCID 86629171 | — |
Reaction Steps
Under ice-cooling, 296 mg of sodium hydride was added to an N,N-dimethylformamide solution (30 ml) of 1.99 g N-(3,4-dimethoxyphenyl)benzene sulfonamide and stirred at room temperature for 30 minutes, and then 0.75 ml of ethyl bromoacetate was added thereto and stirred for 2 hours. The reaction liquid was poured into ice water, acidified by adding 1 M hydrochloric acid and then extracted with ethyl acetate. The organic layer was washed with saturated brine, dried with anhydrous sodium sulfate and then concentrated under a reduced pressure. The thus obtained residue was purified by a silica gel column chromatography using ethyl acetate:n-hexane (1:2) as the elution solvent, thereby obtaining 2.47 g of ethyl [(3,4-dimethoxyphenyl)(phenylsulfonyl)amino]acetate as a pale yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101580B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-9a69906a47484961938dd77ff2a73dfa |
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| Source note | uspto-grants-2012_01 |
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