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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379568Generated: October 30, 2026

Hydrochloric Acid → 2,3,4-Trifluoro-5chlorobenzyl alcohol

https://huagongshe.com/reaction/2379568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Chloro-2,3,4-trifluorobenzoyl fluorideHCID 13565015—
Solvent1,4-DioxaneHCID 31275—
Product2,3,4-Trifluoro-5chlorobenzyl alcoholHCID 1356502188.5%

Reaction Steps

62 g of NaBH4 are initially introduced into 320 ml of dioxane. A solution of 319 g of 5-chloro-2,3,4-trifluorobenzoyl fluoride in 640 ml of dioxane is run into this, at the reflux temperature, over the course of 6 hours. After boiling under reflux for a further hour, the mixture is poured onto ice, the pH is adjusted to 1 with dilute hydrochloric acid, and the organic phase is extracted with methylene chloride and then distilled: 261 g of 2,3,4-trifluoro-5-chlorobenzyl alcohol of boiling point 109° C./12 mbar are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05362909
Source datasetuspto-grants-1994_11
ORD IDord-30fd8f6ca4c2474288e10a7464af050d
Source noteuspto-grants-1994_11