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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073253Generated: October 26, 2026

Potassium sodium tartarate → (2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-formylpyrrolidine

https://huagongshe.com/reaction/2073253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium sodium tartarateHCID 9855836—
Reactant(2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-methoxycarbonylpyrrolidineHCID 14772685—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product(2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-formylpyrrolidineHCID 1567037765.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-methoxycarbonylpyrrolidine (9.01 g) in toluene (70 ml) was added dropwise 1.5 molar solution of diisobutylaluminum hydride (61.2 m mol) in tetrahydrofuran (40.8 ml) at -78° C. After the mixture was stirred at -78° C. for 1.5 hours, saturated aqueous potassium sodium tartrate was added to the reaction mixture and the mixture was filtered through Celite. The solid was washed with ethyl acetate and the combined organic solution was washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was chromatographed on a silica gel column with a mixture of ethyl acetate and n-hexane (1:2-2:1) as an eluent to give (2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-formylpyrrolidine (5.51 g) as pale yellow crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04916152
Source datasetuspto-grants-1990_04
ORD IDord-1615f33cf72341f1b70f465910f68ced
Source noteuspto-grants-1990_04