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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065603Generated: October 31, 2026

Hydrochloric Acid → HCID 54346943, compound

https://huagongshe.com/reaction/1065603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant3,5-Dichloro-2,4,6-trifluorobenzoyl fluorideHCID 19850482—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 54346943HCID 54346943—

Reaction Conditions

Temperature20 °C

Reaction Steps

400 ml of dry dioxane and 55 g of sodium borohydride are initially introduced into a 2 l three-necked flask with a stirrer, reflux condenser and dropping funnel at 20° C., and 247 g of 3,5-dichloro-2,4,6-trifluorobenzoyl fluoride, dissolved in 250 ml of dry dioxane, are then added dropwise at this temperature. When the addition has ended, the mixture is stirred at 20° C. for a further 2 hours and then warmed to the reflux temperature for 1 hour. The solution is cooled to room temperature, a total of 50 ml of water are then added dropwise and the mixture is subsequently rendered acid with dilute hydrochloric acid. The reaction mixture is extracted three times with methylene chloride and, after drying the organic phase over sodium sulphate, the solvent is distilled off. 196.5 g (85% of the theoretical yield) of 3,5-dichloro-2,4,6-trifluorobenzyl alcohol of boiling point 134° to 135° C./20 mbars and melting point 67° to 68° C. are obtained from the residue by further distillation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04330366
Source datasetuspto-grants-1982_05
ORD IDord-666aa7aec3a74cdba2fbc0354c04de4b
Source noteuspto-grants-1982_05