HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597620Generated: October 25, 2026
(-)-Asparagine → N-Phenysulfonyl-L-asparagine
https://huagongshe.com/reaction/1597620
Participants
| Role | Name | HCID | Charge |
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| Reactant | (-)-Asparagine | HCID 6267 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Phenysulfonyl-L-asparagine | HCID 10754635 | — |
Reaction Steps
To a stirred solution of L-asparagine (Aldrich) (10 g, 76 mmol), NaOH (3.4 g, 85 mmol), H2O (50 mL), and dioxane (50 mL) at 0° C. was added PhSO2Cl (10.6 mL, 84 mmol). After 1 min, NaOH (3.4 g) in H2O (50 mL) was added and the reaction mixture stirred for 30 min. The reaction mixture was then concentrated to remove the dioxane then washed with EtOAc. The aqueous phase was then cooled to 0° C. and acidified to pH 5.0 with conc. HCl to effect product precipitation. The resulting solid was collected by filtration, washed with H2O (20 mL) and dried at 50° C. under vacuum to give N-phenylsulfonyl-L-asparagine (1-1a) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06294549B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-2a8a9ae9b6494bceb0e54b5c40b7a588 |
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| Source note | uspto-grants-2001_09 |
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