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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166753Generated: October 26, 2026

m-Chloroperbenzoic acid → N-BOC 1-amino-2-chloro-3-(p-nitrophenyl)sulfinylpropane

https://huagongshe.com/reaction/2166753

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantN-BOC 1-amino-2-chloro-3-(p-nitrophenyl)thiopropaneHCID 13135212—
SolventDichloromethaneHCID 6344—
ProductN-BOC 1-amino-2-chloro-3-(p-nitrophenyl)sulfinylpropaneHCID 53988848—

Reaction Conditions

Temperature25 °C

Reaction Steps

The product from Step B, 2.II, 207 mg, in 9 ml of CH2Cl2 is treated dropwise at 0° C. over 70 minutes with 121 mg of m-chloroperbenzoic acid (MCPBA) (85%) in 9 ml of CH2Cl2 under N2. The solution is stirred 1 hour at 25° C., washed with aqueous NaHCO3, dried with MgSO4, filtered, evaporated (209 mg) and purified by preparative thin layer chromatography on silica gel with 4:1 (v/v) CHCl3 -ethylacetate, affording 97 mg of pure product, Rf 0.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04388475
Source datasetuspto-grants-1983_06
ORD IDord-7402f6d22c854e3f8c9621e4348c0756
Source noteuspto-grants-1983_06