HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742058Generated: October 26, 2026
4-Methoxybenzenesulfonyl chloride → N-[4-methoxybenzenesulfonyl]-(D)-asparagine
https://huagongshe.com/reaction/742058
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | D-Asparagine | HCID 439600 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-[4-methoxybenzenesulfonyl]-(D)-asparagine | HCID 27014145 | — |
Reaction Steps
D-asparagine (13.2 g, 100.0 mmol) is dissolved in dioxane (75.0 mL) and water (125.0 mL), triethylamine (21.0 mL, 150.0 mmol) is added, and the solution is cooled to 0° C. To this solution is added 4-methoxybenzenesulfonyl chloride (22.7 g, 110.0 mmol) over 10 minutes. The reaction is warmed to room temperature and stirred for 3 days. The precipitate is then filtered off, the filtrate is acidified to pH=~4, and extracted well with ethyl acetate. A first crop of pure product precipitates from the ethyl acetate and is collected by filtration. A second crop is obtained by evaporating off the ethyl acetate, and rinsing the solid obtained with water to remove inorganic salts. The two crops are combined to give N-[4-methoxybenzenesulfonyl]-(D)-asparagine.
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-1994d66083674cf799c8b45050933a17 |
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| Source note | uspto-grants-1996_09 |
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