Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182052Generated: October 26, 2026

Isoamylamine → 2-Bromo-4-((isopentylamino)methyl)phenol

https://huagongshe.com/reaction/1182052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamylamineHCID 7894—
Reactant3-Bromo-4-hydroxybenzaldehydeHCID 76308—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product2-Bromo-4-((isopentylamino)methyl)phenolHCID 5893800475%

Reaction Steps

Combine 3-Bromo-4-hydroxy-benzaldehyde (1.5 g, 7.5 mmol) with 3-methylbutylamine (867 μL, 7.5 mmol), MeOH (25 mL) and molecular sieves 3A (5.8 g) and stir at room temperature overnight. Add NaBH4 (1.4 g, 37.3 mmol) and stir at room temperature for 2 hours. Filtrate over celite with MeOH and eliminate the solvent. Purify by SCX ion-exchange chromatography to afford the title compound (1.5 g, 75%). 1H-NMR (CD3OD, 300 MHz): 7.52 (d, 1H, J=2.0 Hz), 7.17 (dd, 1H, J=2.0 and 8.5 Hz), 6.87 (d, 1H, J=8.5 Hz), 3.80 (s, 2H), 2.79-2.74 (m, 2H), 1.76-1.63 (m, 1H), 1.54 (q, 2H, J=6.8 Hz), 0.99 (d, 6H, J=6.56 Hz). 13C-NMR (CD3OD, 300 MHz): 158.6, 134.9, 130.7, 128.6, 118.8, 112.7, 53.3, 47.9, 38.6, 27.8, 23.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288543B2
Source datasetuspto-grants-2007_10
ORD IDord-2b5bfd974d79454992ee8e699bfd331b
Source noteuspto-grants-2007_10