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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 2-Iodo-5-(trifluoromethyl)benzoic acid | HCID 18451533 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Iodo-5-(trifluoromethyl)phenyl)methanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781426B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-23c1ac6ac681465da7135c5ec2512b9a |
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| Source note | uspto-grants-2010_08 |
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