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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189949Generated: October 29, 2026

HCID 19762862, compound → HCID 67296566, compound

https://huagongshe.com/reaction/1189949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19762862HCID 19762862—
Reactant3-(3-Aminophenyl)-3-hydroxypropanenitrileHCID 59316960—
SolventWater ethanolHCID 19096565—
ProductHCID 67296566HCID 67296566—

Reaction Steps

To a stirred solution of aniline 12 (1.0 g, 6.1 mmol) in EtOH:H2O (9:1) was added 2-propylpentyl 4-methylbenzenesulfonate (0.87 g, 3.08 mmol). The reaction mixture was heated under reflux for 4 days, concentrated under reduced pressure. The residue was diluted with water and extracted with EtOAc three times. Combined organic layers were dried over anhydrous sodium sulfate and concentrated under reduced pressure to dryness. Purification by flash chromatography (25% EtOAc—hexanes) gave 3-hydroxy-3-(3-(2-propylpentylamino)phenyl)propanenitrile as a colorless semi-solid. Yield (0.3 g, 18%); 1H NMR (400 MHz, CDCl3) δ 7.17 (t, J=7.6 Hz, 1H), 6.66 (d, J=7.6 Hz, 1H), 6.62 (d, J=2.0 Hz, 1H), 6.57 (dd, J=2.0, 8.0 Hz, 1H), 4.95 (dt, J=3.2, 6.0 Hz, 1H), 3.72 (bs, 1H), 3.02 (d, J=6.0 Hz, 2H), 2.80 (d, J=6.8 Hz, 2H), 2.89 (d, J=3.2 Hz, 1H), 1.64-1.57 (m, 1H), 1.37-1.20 (m, 8H), 0.84 (t, J=6.8 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674137B2
Source datasetuspto-grants-2014_03
ORD IDord-51f1b119d05548b68bc690914ca413f5
Source noteuspto-grants-2014_03