HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234855Generated: October 31, 2026
Hydrochloric Acid → HCID 67630140, compound
https://huagongshe.com/reaction/234855
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Naphthalenesulfonyl chloride | HCID 7125 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Amino-4-(benzyloxy)-4-oxobutanoic acid | HCID 351981 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67630140 | HCID 67630140 | 98.4% |
Reaction Steps
22.4 ml of 2N NaOH are added dropwise at 10° C. to a solution of 5 g of D-aspartic acid β-benzyl ester and 5.07 g of 2-naphthylsulphonyl chloride in 80 ml of dioxan cooled to 10° C. The reaction mixture is subsequently stirred at room temperature for 2 hours and then treated with 25 ml of 1N hydrochloric acid. After evaporation of the dioxan the residue is taken up in ethyl acetate and washed with water. After drying and evaporation of the ethyl acetate phase there are obtained 9.1 g of 4-benzyl 1-hydrogen N-(2-naphthylsulfonyl)-D-aspartate, Rf=0.53 (ethyl acetate/glacial acetic acid 0.97:0.03).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05595999 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-1451170c986343c497d707fed09d9c4a |
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| Source note | uspto-grants-1997_01 |
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