Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820148Generated: October 30, 2026

Formaldehyde → N-{2,6-Dimethyl-4-[methyl-(4-trifluoromethyl-benzyl)-amino]-phenyl}-acetamide

https://huagongshe.com/reaction/1820148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-[2,6-Dimethyl-4-(4-trifluoromethyl-benzylamino)-phenyl]-acetamideHCID 11652937—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductN-{2,6-Dimethyl-4-[methyl-(4-trifluoromethyl-benzyl)-amino]-phenyl}-acetamideHCID 1163885260.5%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a stirred solution of N-[2,6-dimethyl-4-(4-trifluoromethyl-benzylamino)-phenyl]-acetamide (4a, 1.0 g) and formaldehyde (1 mL) in methanol (20 mL) and acetic acid (1 mL) was slowly added sodium cyanoborohydride (0.30 g). After 15 minutes, the reaction mixture was cooled to 5° C. for 16 hours to precipitate the product, which was collected by filtration and washed with water (100 mL) to furnish 0.63 g (60% yield) of the title compound as a pale yellow solid. LC-MS-TOF (m/z) 351 (MH+); tR=2.58, (UV, ELSD) 99%, 99%. 1H NMR (500 MHz, DMSO-d6): 1.97 (s, 3H), 2.02 (s, 6H), 2.97 (s, 3H), 4.63 (s, 2H), 7.41 (d, 2H), 7.68 (d, 2H), 8.88 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601870B2
Source datasetuspto-grants-2009_10
ORD IDord-38c97ae7afdd42388d166077af16dfa7
Source noteuspto-grants-2009_10