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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189974Generated: October 31, 2026

Benzaldehyde → 3-(3-(Benzylamino)phenyl)-3-hydroxypropanenitrile

https://huagongshe.com/reaction/1189974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-(3-Aminophenyl)-3-hydroxypropanenitrileHCID 59316960—
SolventDichloromethaneHCID 6344—
Product3-(3-(Benzylamino)phenyl)-3-hydroxypropanenitrileHCID 67296728—

Reaction Steps

NaBH(OAc)3 (7.84 g, 36.99 mmol) was added to a solution of aniline 12 (2.0 g, 12.33 mmol) and benzaldehyde (1.3 g, 12.33 mmol) in DCM. The resulting mixture was stirred at RT for 5 h and quenched with saturated aqueous NaHCO3. Organic layer was washed with water followed by brine and dried over anhydrous Na2SO4. Organic layer was concentrated under reduced pressure. Purification by flash chromatography (40% to 50% EtOAc—hexanes gradient) gave 3-(3-(benzylamino)phenyl)-3-hydroxypropanenitrile as a pale yellow oil. Yield (2.61 g, 83%); 1H NMR (400 MHz, DMSO-d6) δ 7.36-7.29 (m, 4H), 7.23-7.19 (m, 1H), 6.99 (t, J=8.0 Hz, 1H), 6.68 (s, 1H), 6.54 (d, J=7.6 Hz, 1H), 6.44 (dd, J=1.6, 8.0 Hz, 1H), 6.27 (t, J=6.0 Hz, 1H), 5.79 (d, J=4.4 Hz, 1H), 4.72-4.68 (m, 1H), 4.25 (d, J=6.0 Hz, 2H), 2.82-2.67 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674137B2
Source datasetuspto-grants-2014_03
ORD IDord-d23508e709144268b55764c700c95fb6
Source noteuspto-grants-2014_03