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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357309Generated: October 25, 2026

4-(4-(2-Amino-2-methylpropyl)phenoxy)benzamide → (S)-4-(4-[2-(N-[3-(2-amino-3-nitrophenoxy)-2-hydroxypropyl]amino)-2-methylpropyl]phenoxy)benzamide

https://huagongshe.com/reaction/357309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-(2-Amino-2-methylpropyl)phenoxy)benzamideHCID 11832961—
Reactant(S)-3-(2-Amino-3-nitrophenoxy)-1,2-epoxypropaneHCID 15049327—
SolventEthanolHCID 702—
Product(S)-4-(4-[2-(N-[3-(2-amino-3-nitrophenoxy)-2-hydroxypropyl]amino)-2-methylpropyl]phenoxy)benzamideHCID 5404542862%

Reaction Conditions

Temperature55 °C

Reaction Steps

A suspension of (S)-3-(2-amino-3-nitrophenoxy)-1,2-epoxypropane (5 g, 23.8 mmol) and 4-(4-(2-amino-2-methylpropyl)phenoxy)benzamide (20.3 g 71.1 mmol) in absolute ethanol (200 mL) was heated to 55° C. for 12 h. All solids went into solution at 50° C. Upon completion of the reaction, the solvent was evaporated to dryness. The residue was redissolved in ethyl acetate and washed with a saturated solution of sodium bicarbonate. The layers were separated and the aqueous phase was extracted with ethyl acetate. The two organic layers were combined and washed with brine. The phases were separated and the organic layer was dried over sodium sulfate, filtered, and the solvent evaporated. column chromatography eluting with 20% MeOH/CHCl3 gave 7.26 g (62%) of product. NMR. MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840738
Source datasetuspto-grants-1998_11
ORD IDord-799b432b234448928455bc3574ac0dc9
Source noteuspto-grants-1998_11