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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505268Generated: October 25, 2026

Borane;tetrahydrofuran → (2-Iodo-5-(trifluoromethyl)phenyl)methanol

https://huagongshe.com/reaction/505268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant2-Iodo-5-(trifluoromethyl)benzoic acidHCID 18451533—
SolventTetrahydrofuranHCID 8028—
Product(2-Iodo-5-(trifluoromethyl)phenyl)methanolHCID 23160665—

Reaction Steps

Borane-THF (11.0M solution in THF; 94 mL; 94 mmol) was added to a stirred solution of 2-iodo-5-(trifluoromethyl)benzoic acid (Intermediate 9, 2.97 g; 9.4 mmol) in THF (300 mL) at 0° C. under N2. The reaction was heated at reflux for 90 min and then carefully quenched with 6N HCl until no further gas evolution. The reaction was diluted with H2O (250 mL) and extracted with EtOAc (3×250 mL). The combined extracts were washed with brine (300 mL), dried over MgSO4, filtered, and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel (0-25% EtOAc/hexanes gradient) to afford [2-iodo-5-(trifluoromethyl)phenyl]methanol as a white solid. LCMS=285.0 (M−17)+. 1H NMR (CDCl3, 500 MHz): δ 7.97 (d, J=8.3 Hz, 1 H), 7.79 (s, 1 H), 7.28 (d, J=8.4 Hz, 1 H), 4.75 (s, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781426B2
Source datasetuspto-grants-2010_08
ORD IDord-23c1ac6ac681465da7135c5ec2512b9a
Source noteuspto-grants-2010_08