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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371048Generated: October 26, 2026

Water → 3-Bromo-4-(trifluoromethoxy)benzaldehyde

https://huagongshe.com/reaction/371048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium DichromateHCID 24502—
Reactant3-Bromo-4-(trifluoromethoxy)benzyl alcoholHCID 26597851—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventDichloromethaneHCID 6344—
Product3-Bromo-4-(trifluoromethoxy)benzaldehydeHCID 1315041675.8%

Reaction Steps

A mixture of 29.4 g (0.3 mol) of sulphuric acid, 50 ml of water and 2 ml of "Aliquat" 336 (tricaprylmethylammonium chloride) was added to a solution of 27 g (0.1 mol) of 3-bromo-4-trifluoromethoxybenzyl alcohol in 250 ml of methylene chloride at room temperature. Thereafter, 9.7 g (0.033 mol) of potassium dichromate were added to the reaction mixture, and the temperature was kept at approx. 25° C. for 2 hours by slight cooling. After 100 ml of water had been added to the mixture, the organic phase was separated off and the water was once again extracted by shaking with 100 ml of methylene chloride. The organic phases were washed twice with 100 ml of water, then once with 100 ml of saturated sodium bicarbonate solution, and once again with 100 ml of water, dried over sodium sulphate, and concentrated by evaporation in vacuo. The residue was distilled. In this manner, 20.4 g (75.8% of theory) of 3-bromo-4-trifluoromethoxybenzaldehyde were obtained as a colorless oil of boiling point 97° C./10 mm Hg. ##STR23##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04529557
Source datasetuspto-grants-1985_07
ORD IDord-ec6cce784a0947adbcaba56caf913641
Source noteuspto-grants-1985_07