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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
ReactantHCID 86590872HCID 86590872—
SolventDimethylformamideHCID 6228—
Product(3S)-3-acetoxy-1-(p-nitrobenzyloxycarbonyl)pyrrolidineHCID 6954412482%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-6b48b65dc6cd428d91903a33c8752df8
Source noteuspto-grants-2006_02