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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474566Generated: October 30, 2026

Methylamine → [(4-{[4-Chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]methylamine

https://huagongshe.com/reaction/474566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(4-Chloro-3-(trifluoromethyl)phenoxy)benzaldehydeHCID 86666187—
Product[(4-{[4-Chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]methylamineHCID 67776010—

Reaction Conditions

Temperature23 °C

Reaction Steps

4-{[4-Chloro-3-(trifluoromethyl)phenyl]oxy}benzaldehyde (3 g, 9.98 mmol) was mixed with a methylamine (1.549 g, 49.9 mmol) alcohol solution. The reaction mixture was stirred at 23° C. overnight. NaBH4 (1.132 g, 29.9 mmol) was added and stirred for additional 2 h. Purification via an ISCO system then provided the title compound as a yellow solid. LCMS: rt=2.53 min, [M+H+]=316.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-3a400964b43042fa9ad14d40c3dd0807
Source noteuspto-grants-2014_01