Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82962Generated: October 25, 2026

Water → 1-(Diphenylmethyl)-3-(pentylsulfonyl)azetidine

https://huagongshe.com/reaction/82962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant1-(Diphenylmethyl)-3-(pentylthio)azetidineHCID 67154644—
SolventMethanolHCID 887—
Product1-(Diphenylmethyl)-3-(pentylsulfonyl)azetidineHCID 6715459430%

Reaction Steps

To a solution of 1-(diphenylmethyl)-3-(pentylthio)azetidine (228 mg, 0.70 mmol; which may be prepared as described in Step 2) in methanol (6.3 mL) and water (6.3 mL) was added H2SO4 1N (0.7 mL). The reaction mixture was stirred for 10 minutes, then oxone (1.08 g, 1.75 mmol) was added and the mixture stirred at room temperature for 12 h. A solution of saturated NaHCO3 (5 mL) was added and the mixture extracted with ethyl acetate. The two layers were separated and the organic washed with brine, dried over Na2SO4, filtered and concentrated. The crude was then purified on column chromatography (pentane/EtOAc, 100/0 then 90/10) to give the title product (75 mg, 30%) as a pale yellow oil. The less pure fraction (N-oxide) can be recycled in hydrogenolysis conditions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846711B2
Source datasetuspto-grants-2014_09
ORD IDord-f630a1a4c82748fa9814874697e5c059
Source noteuspto-grants-2014_09