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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725117Generated: November 1, 2026

tert-Butyl hydroperoxide → N-Benzyloxycarbonyl-4-[(R*)-2-methyl-sulfinylphenyl]piperidine

https://huagongshe.com/reaction/725117

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
Reactant1-Benzyloxycarbonyl-4(2-methylthiophenyl)piperidineHCID 11110620—
Reactantdiethyl-D-tartarateHCID 29414049—
ReactantN-Benzyloxycarbonyl-4-[(R*)-2-methylsulfinylphenyl]-piperidineHCID 53634760—
CatalystTitanium isopropoxideHCID 11026—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-Benzyloxycarbonyl-4-[(R*)-2-methyl-sulfinylphenyl]piperidineHCID 86750107—

Reaction Conditions

Temperature-15 °C

Reaction Steps

N-Benzyloxycarbonyl-4-[(R*)-2-methylsulfinylphenyl]-piperidine. To a solution of diethyl-D-tartarate (3.4 mL) in dichloromethane (50 mL) was added titanium tetraisopropoxide (3.0 mL) followed by water (0.18 mL). The resulting solution was stirred vigorously for 30 minutes, treated with N-benzyloxycarbony-4-(2-methylthiophenyl)piperidine (3.41 g), and cooled to -15° C. The reaction mixture was treated with tert-butylhydroperoxide (2 mL) drop wise over a period of 1 minute, and stirred at -15° C. for 40 hours. Water (4 mL) was added, and the solution was stirred vigorously for 1 hour and filtered through a bed of diatomous earth. The filtrate was stirred with 5% aqueous sodium hydroxide (100 mL) for 1 hour and was washed with brine (50 mL). The aqueous layer was extracted with dichloromethane and the combined organic layers were washed (brine), dried (anhydrous sodium sulfate), and evaporated to give a solid product which was crystallized from diisopropyl ether to afford N-Benzyloxycarbonyl-4-[(R*)-2-methyl-sulfinylphenyl]piperidine (3.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705505
Source datasetuspto-grants-1998_01
ORD IDord-b6a183ac64894400abc97e4047a78ba0
Source noteuspto-grants-1998_01