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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744888Generated: October 31, 2026

Sodium hydride → HCID 57266598, compound

https://huagongshe.com/reaction/744888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 57114913HCID 57114913—
ReactantHCID 178526132HCID 178526132—
SolventSodium IodideHCID 5238—
SolventDimethylformamideHCID 6228—
ProductHCID 57266598HCID 5726659870.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

Next, 36.4 g of thiobenzoic acid was dissolved in 300 ml of dimethylformamide and cooled on an ice bath, to which was subsequently added 10.5 g of sodium hydride. To this were added 102 g of (2S,4R)-1-(t-butoxycarbonyl)-2-ethoxycarbonyl -4-(p-toluenesulfonyloxy)pyrrolidine dissolved in 200 ml of dimethylformamide and 37.5 g of sodium iodide, followed by heating at 80° C. for 3 hours. After concentration of the reaction mixture, the thus obtained residue was dissolved in .benzene, and the resulting organic layer was washed with 5% sodium bicarbonate aqueous solution, 10% citric acid aqueous solution and water in that order, followed by drying over sodium sulfate and subsequent evaporation of the solvent under a reduced pressure. The resulting residue was purified by a silica gel column chromatography to yield 66 g of (2S,4S)-1-(t-butoxycarbonyl)-2-ethoxycarbonyl -4-benzoylthiopyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559224
Source datasetuspto-grants-1996_09
ORD IDord-f7b80768ff7d46eebdd05d5ea9a31630
Source noteuspto-grants-1996_09