HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742049Generated: October 29, 2026
4-Methoxybenzenesulfonyl chloride → HCID 3113410, compound
https://huagongshe.com/reaction/742049
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 3113410 | HCID 3113410 | — |
Reaction Steps
Glycine ethyl ester hydrochloride (31.39 g, 225.0 mmol) is dissolved in dioxane (150 mL) and water (150 mL), triethylamine (69.0 mL, 495.0 mmol) is added, and the solution is cooled to 0° C. To this solution is added 4-methoxybenzenesulfonyl chloride (51.15 g, 248.0 mmol) over 10 minutes. The reaction is warmed to room temperature and stirred overnight. The next day the mixture is reduced to one-half volume by evaporating solvent, diluted with 1N sodium hydroxide, and extracted well with ether. The combined organic layers are washed with brine, dried (Na2SO4), and the solvent is evaporated. The product is recrystallized from ether/ethyl acetate/hexanes to give ethyl 2-[[4-methoxybenzenesulfonyl]amino]acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05552419 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-9d72ea1824904a9baaea46182f13b4ca |
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| Source note | uspto-grants-1996_09 |
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