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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012199Generated: October 29, 2026

Vanillin → 4-((2,4-BIS(TRIFLUOROMETHYL)BENZYL)OXY)-3-METHOXYBENZALDEHYDE

https://huagongshe.com/reaction/1012199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVanillinHCID 1183—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-Bis(trifluoromethyl)benzyl bromideHCID 518871—
SolventEthyl AcetateHCID 8857—
Product4-((2,4-BIS(TRIFLUOROMETHYL)BENZYL)OXY)-3-METHOXYBENZALDEHYDEHCID 11383352100.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a flask was added 1-bromomethyl-2,4-bis-trifluoromethyl-benzene (2.27 g, 7.39 mmol), vanillin (1.12 g, 1 equiv), DMF (23 mL) and fine mesh K2CO3 (5.11 g, 37 mmol). The reaction slurry was stirred at 70° C. for 15 h. The reaction solution was diluted with EtOAc (120 mL), filtered through a Buchner funnel, washed with sat NH4Cl (50 mL×2), dried over Na2SO4, filtered, and concentrated. The crude material was chromatographed (SiO2, Hex/EtOAc: 100:0 to 70:30) to yield intermediate product (2.79 g, 86%). 1H NMR (400 MHz, CDCl3) δ 9.88 (s, 1H), 7.97 (d, J=8 Hz, 1H), 7.96 (s, 1H), 7.85 (d, J=8 Hz, 1H), 7.48 (s, 1H), 7.42 (d, J=8 Hz, 1H), 6.93 (d, J=8 Hz, 1H), 5.48 (s, 2H), 3.99 (s, 3H); MS (ESI) 379 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977489B2
Source datasetuspto-grants-2011_07
ORD IDord-8ce01345b1a64f3589f3b314349069de
Source noteuspto-grants-2011_07