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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558579Generated: October 29, 2026

4-Methoxybenzylamine → (4-Methoxy-benzyl)-(3-trifluoromethyl-pyridin-2-yl)-amine

https://huagongshe.com/reaction/558579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-3-(trifluoromethyl)pyridineHCID 589833—
Solvent1-ButanolHCID 263—
Product(4-Methoxy-benzyl)-(3-trifluoromethyl-pyridin-2-yl)-amineHCID 2955856983.1%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of commercially available 2-chloro-3-trifluoromethylpyridine (64.83 g, 357 mmol), 4-methoxybenzylamine (56 mL, 429 mmol) and DIPEA (73.4 mL, 429 mmol) in n-butanol (100 mL) was refluxed (oil bath temp. 140° C.) for 3.5 days. Concentrated in vacuum, partitioned between 25% HCl and TBME, reextracted the organic layer twice with 25% HCl, the aqueous layer was made alkaline with 32% NaOH, extracted with TBME, washed with brine and dried over Na2SO4. Removal of the solvent in vacuum left a brown oil (105.21 g, >100%). Vacuum distillation gave the product as a colorless liquid (83.766 g, 83%, bp 139-141° C. at 1.4 mbar). MS (ISP) 283.1 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063048B2
Source datasetuspto-grants-2011_11
ORD IDord-1645d5c269ce45ecb5b88106a23ab995
Source noteuspto-grants-2011_11