Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994501Generated: October 30, 2026

Hydrochloric Acid → (2-Iodo-5-(trifluoromethyl)phenyl)methanol

https://huagongshe.com/reaction/1994501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Iodo-5-(trifluoromethyl)benzaldehydeHCID 71650906—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(2-Iodo-5-(trifluoromethyl)phenyl)methanolHCID 23160665—

Reaction Steps

An alternative procedure is as follows: To a solution of 2-Iodo-5-(trifluoromethyl)benzaldehyde (EXAMPLE 80, Step A, 9 g) in THF (100 mL) and water (10 mL) at 0° C. was added NaBH4 (0.5 g). The reaction was stirred 30 minutes. To the reaction mixture was added dilute aqueous HCl (cautiously). The mixture was extracted with ether and the ether layer was washed with water, then brine. The ether layer was then dried over anhydrous MgSO4, filtered and concentrated. The material is chromatographed on SiO2 using a step gradient of 1:3 CH2Cl2/hexanes, then 1:1 CH2Cl2/hexanes, then 100% CH2Cl2 to afford [2-iodo-5-(trifluoromethyl)phenyl]methanol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652049B2
Source datasetuspto-grants-2010_01
ORD IDord-0e68aac6d87f4764bb14a7dd2824286c
Source noteuspto-grants-2010_01