HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250759Generated: October 25, 2026
Hydrochloric Acid → [2,6-Bis(trifluoromethyl)phenyl]methanol
https://huagongshe.com/reaction/250759
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Benzene, 1,3-bis(trifluoromethyl)- | HCID 223106 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2,6-Bis(trifluoromethyl)phenyl]methanol | HCID 15346431 | 41% |
Reaction Steps
A mixture of 80 mL of THF and t-BuOK (7.0 g, 62.5 mmol) is added to a 250 mL four-neck flask equipped with a mechanical stirrer, a thermometer, a gas inlet tube and a 100 mL dropping funnel with a gas outlet tube. Cool down to −70° C. and 2,6-bis(trifluoromethyl)benzene (8.0 mL, 10.7 g, 50.0 mmol) is added dropwise and keep agitating ˜−70° C. for 30 min. Add n-BuLi (0.10 mol, 2.87 M in hexanes 35.0 mL, 100.0 mmol) dropwise over 30 min with agitation at ˜−70° C. for 60 min. Paraformaldehyde (6.0 g, 0.20 mol) is added and keep agitating ˜70° C. for 30 min, then gradually warm to room temperature for 3 h. Pour mixture into conc HCl (10 mL) and ice water (300 mL), and stir for 1 h. Extract with hexanes (3×50 mL). Wash the combined organic layers with 50 mL of brine, dry over anhydrous Na2SO4, filter and concentrate. The crude product is vacuum distilled (72-76° C. at 4-5 mm Hg) to give the desired compound (5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863310B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-da2d5e34cdd941ddb07bf7cd82e3089f |
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| Source note | uspto-grants-2011_01 |
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