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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4-Bis(trifluoromethyl)benzyl bromide | HCID 518871 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-((2,4-BIS(TRIFLUOROMETHYL)BENZYL)OXY)-3-METHOXYBENZALDEHYDE | HCID 11383352 | 100.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977489B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-8ce01345b1a64f3589f3b314349069de |
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| Source note | uspto-grants-2011_07 |
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