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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252233Generated: November 1, 2026

Methyl (methylsulfinyl)methyl sulfide → 1-p-Nitrobenzyloxycarbonyl-4-hydroxy-4-methylsulfinylmethylthiomethylpiperidine

https://huagongshe.com/reaction/1252233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl (methylsulfinyl)methyl sulfideHCID 99129—
Reactant(4-Nitrophenyl)methyl 4-oxopiperidine-1-carboxylateHCID 13292708—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-p-Nitrobenzyloxycarbonyl-4-hydroxy-4-methylsulfinylmethylthiomethylpiperidineHCID 57134009—

Reaction Steps

To methyl methylthiomethyl sulfoxide (2.23 g) in dry tetrahydrofuran (10 ml) was added dropwise n-butyl lithium (1.15 g) in dry hexane (11.6 ml) at -60° to -70° C. under nitrogen atmosphere and the mixture was stirred for 20 minutes at the same temperature. Subsequently, 1-p-nitrobenzyloxycarbonyl-4-piperidone (5.0 g) in dry tetrahydrofuran (30 ml) was added dropwise thereto at -55° to -70° C. under nitrogen atmosphere. The reaction mixture was diluted with dichloromethane (200 ml) and water (215 ml), warmed slowly to room temperature, dried over anhydrous sodium sulfate and evaporated to give an oily residue which was then purified by silica gel chromatography to give 1-p-nitrobenzyloxycarbonyl-4-hydroxy-4-methylsulfinylmethylthiomethylpiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742052
Source datasetuspto-grants-1988_05
ORD IDord-f2e618b6c3ab4ebdb1878a655134e8a7
Source noteuspto-grants-1988_05