Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058553Generated: October 26, 2026

2,4-Dichlorobenzyl chloride → 2,4-Dichlorobenzyl alcohol

https://huagongshe.com/reaction/2058553

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichlorobenzyl chlorideHCID 7212—
Reactant2,4-DichlorotolueneHCID 7254—
Reactant2,4-Dichloro-1-(dichloromethyl)benzeneHCID 8637—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
Product2,4-DichlorotolueneHCID 725411.84%
Product2,4-DichlorobenzaldehydeHCID 1340416.94%
Product2,4-Dichlorobenzyl alcoholHCID 1568471.21%

Reaction Conditions

Temperature160 °C

Reaction Steps

To a 600 cc Hastoloy C autoclave was charged 48.52 g of a crude chlorination mixture containing 10.93% 2,4-dichlorotoluene, 70.39% α,2,4-trichlorotoluene, 18.52% α,α,2,4-tetrachlorotoluene, 0.10% α,α,2,4-pentachlorotoluene (the percentages represent gas chromatograph area percents), 39 g of sodium bicarbonate and 146 ml of water. The autoclave was flushed with nitrogen and pressure tested to 1500 psig. The autoclave was then vented to atmospheric pressure and heated. The temperature was increased to 160° C. and maintained for two hours. The pressure increased from atmosphere pressure to between 200 and 400 psig. After two hours, the autoclave was cooled to 80° C., vented and the product removed. After separation of the aqueous phase, the crude aldehyde mixture was flash distilled affording 11.84% 2,4-dichlorotoluene, 16.94% 2,4-dichlorobenzaldehyde and 71.21% 2,4-dichlorobenzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04317934
Source datasetuspto-grants-1982_03
ORD IDord-08541278214043bc831c91b6bc57fb60
Source noteuspto-grants-1982_03