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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629757Generated: October 31, 2026

4-Hydroxybenzaldehyde → 4-(4,4,4-Trifluorobutoxy)benzaldehyde

https://huagongshe.com/reaction/1629757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantTriphenylphosphineHCID 11776—
Reactant4,4,4-Trifluorobutan-1-olHCID 136307—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
SolventDichloromethaneHCID 6344—
Product4-(4,4,4-Trifluorobutoxy)benzaldehydeHCID 5372478871%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-hydroxybenzaldehyde (20 g, 164 mmol) and 4,4,4-trifluorobutan-1-ol (25 g, 195 mmol) in anhydrous CH2Cl2 (500 mL) at 0° C. under Ar was added a solution of PPh3 (51.5 g, 196 mmol) in CH2Cl2 (200 mL) over 15 min, and then DIAD (36.4 g, 180 mmol) in anhydrous CH2Cl2 (150 mL) was added dropwise. The mixture was stirred at 0° C. for 0.5 h. The reaction was warmed to rt and stirred for another 3 h. The solvent was removed in vacuo and the residue was triturated with CH2Cl2 three times to remove insoluble solids. The combined CH2Cl2 washings were concentrated and the residue was purified by silica gel chromatography (330 g silica gel, eluted with EtOAc in hexanes) to provide Intermediate 2A (27 g, 71%) as a light brown oil. LCMS Anal. Calc'd for C11H11F3O2 232.20, found [M+H] 233.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791091B2
Source datasetuspto-grants-2014_07
ORD IDord-4253b1626534403ba673b7dd1a275090
Source noteuspto-grants-2014_07