HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346343Generated: October 30, 2026
Thiobenzoic Acid → (2S,4S)-4-benzoylthio-2-(carbamoylmethyl)thiomethyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidine
https://huagongshe.com/reaction/346343
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiobenzoic Acid | HCID 7414 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (2S,4R)-2-(carbamoylmethyl)thiomethyl-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine | HCID 18641550 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2S,4S)-4-benzoylthio-2-(carbamoylmethyl)thiomethyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidine | HCID 57081613 | — |
Reaction Steps
To a suspension of sodium hydride (62.8% in oil) (0.22 g) in N,N-dimethylformamide (5 ml) was added dropwise thiobenzoic S-acid (0.66 ml) under ice-cooling. After stirring under the same condition for 30 minutes, this solution was added to a solution of (2S,4R)-2-(carbamoylmethyl)thiomethyl-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (1.68 g) in N,N-dimethylformamide (20 ml) at ambient temperature. The mixture was stirred at 70°-80° C. for 1 hour. The reaction mixture was poured into ice-water (50 ml) and extracted twice with ethyl acetate (50 ml). The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo t.o give a residue. The residue was chromatographed on silica gel (100 g) eluting with a mixture of dichloromethane and acetone (5:1, V/V). The fractions containing the desired compound were collected and evaporated in vacuo to give (2S,4S)-4-benzoylthio-2-(carbamoylmethyl)thiomethyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (0.87 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05061804 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-6a0721e1af3e4bbb932af631deafac5a |
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| Source note | uspto-grants-1991_10 |
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