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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601455Generated: October 31, 2026

Dibenzylamine → (S)-[3-(N,N-Dibenzylamino)-2-hydroxypropoxy]-2-amino-3-nitrobenzene

https://huagongshe.com/reaction/1601455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzylamineHCID 7656—
Reactant(S)-3-(2-Amino-3-nitrophenoxy)-1,2-epoxypropaneHCID 15049327—
SolventMethanolHCID 887—
Product(S)-[3-(N,N-Dibenzylamino)-2-hydroxypropoxy]-2-amino-3-nitrobenzeneHCID 5423252678%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-3-(2-Amino-3-nitrophenoxy)-1,2-epoxypropane (8.0 g, 38.1 mmol) was dissolved in 250 mL of methanol and treated with dibenzylamine (8.05 mL, 42.0 mmol, d=1.026). The mixture was stirred at reflux for 10 hours and then cooled to 0° C. The resulting orange precipitate was filtered and washed with cold methanol, then dried to yield 12.1 g (78%) of a pale orange solid that was pure by NMR and TLC analysis. The material was used without further purification. NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977154
Source datasetuspto-grants-1999_11
ORD IDord-527456c67cb94b369477cacdfb587875
Source noteuspto-grants-1999_11