HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891725Generated: October 28, 2026
Potassium Acetate → (3S)-3-acetoxy-1-(p-nitrobenzyloxycarbonyl)pyrrolidine
https://huagongshe.com/reaction/891725
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 86590872 | HCID 86590872 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (3S)-3-acetoxy-1-(p-nitrobenzyloxycarbonyl)pyrrolidine | HCID 69544124 | 82% |
Reaction Steps
To a solution of (3R)-3-methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)pyrrolidine (7.50 g, 21.8 mmol) (obtained as described in Reference Example 52(2)) in dimethylformamide (225 ml) was added potassium acetate (6.41 g, 65.3 mmol), and the mixture was stirred in an oil bath (80° C.) overnight. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium hydrogencarbonate solution. The organic layer was washed successively with 10% aqueous sodium chloride solution and saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The obtained residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (2:1→1:2) as the eluant to afford (3S)-3-acetoxy-1-(p-nitrobenzyloxycarbonyl)pyrrolidine (5.51 g, yield 82%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001897B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-6b48b65dc6cd428d91903a33c8752df8 |
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| Source note | uspto-grants-2006_02 |
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