HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725936Generated: October 30, 2026
Hydrochloric Acid → HCID 86751885, compound
https://huagongshe.com/reaction/725936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86751886 | HCID 86751886 | — |
| Solvent | Tetrahydrofurfuryl alcohol | HCID 7360 | — |
| Product | HCID 86751885 | HCID 86751885 | — |
Reaction Steps
To a solution of (2S,4S)-4-acetylthio-N-(p-nitrobenzyloxycarbonyl)-2-[4-[N-(p-nitrobenzyloxycarbonyl)aminomethyl]phenethyl]pyrrolidine (495 mg, 0.777 mmol) in tetrahydrofuran-methanol (2:1, 15 ml), 1N aqueous sodium hydroxide (1.5 ml, 1.5 mmol) was added in a nitrogen stream under cooling with ice. After this reaction solution was stirred at the same temperature for 2 hours, 1N aqueous hydrochloric acid (2.0 ml, 2.0 mmol) was added thereto, and this mixed solution was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. The solvent was distilled off in vacuo to give a crude product of (2R,4S)-4-mercapto-N-(p-nitrobenzyloxycarbonyl)-2-[4-[N-(p-nitrobenzyloxycarbonyl)aminomethyl]phenethyl]-pyrrolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05707987 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-a4b8117fd4f848e8b6b9740b606885c5 |
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| Source note | uspto-grants-1998_01 |
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