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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553403Generated: October 26, 2026

Methanol → 3-(2-Nitrobenzylamino)-1-phenylpropanol

https://huagongshe.com/reaction/553403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3-hydroxy-N-(2-nitrobenzyl)-3-phenyl propionic acid amideHCID 67461894—
ReactantHCID 178419153HCID 178419153—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Nitrobenzylamino)-1-phenylpropanolHCID 67461475—

Reaction Steps

3-Hydroxy-N-(2-nitrobenzyl)-3-phenyl propionic acid amide (3.19 g, 10.6 mmol) was dissolved in tetrahydrofuran (50 ml) and under ice cooled condition, 1 M tetrahydrofuran-borane tetrahydrofuran solution (27.0 ml, 27.0 mmol) was added dropwise thereto. After the dropwise addition was finished, the reaction mixture was returned to room temperature and stirred for one hour, then heated to reflux for six hours and allowed to cool. Methanol (30 ml) was added thereto under ice cooled condition and heated to reflux for 30 minutes. After allowed to cool, the solvent was evaporated and 0.5 N hydrochloric acid water (30 ml) was added. After extracted with diethyl ether, the aqueous layer was adjusted to pH 8 with a saturated sodium hydrogen carbonate aqueous solution and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to obtain 3-(2-nitrobenzylamino)-1-phenylpropanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048825B2
Source datasetuspto-grants-2011_11
ORD IDord-7cf58015a401428da346147e801bd328
Source noteuspto-grants-2011_11