HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509861Generated: October 30, 2026
Tetrahydrofuran → (4,4-Difluorocyclohexyl)methanol
https://huagongshe.com/reaction/1509861
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl-4,4-difluorocyclohexane carboxylate | HCID 2779138 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (4,4-Difluorocyclohexyl)methanol | HCID 21184133 | — |
Reaction Steps
To a solution of 4,4-difluorocyclohexanecarboxylic acid ethyl ester (150 mg, 0.78 mmol) in diethylether (5 mL) at 0° C. was added a 2 M solution of lithium aluminum hydride in THF (0.39 mL, 0.78 mmol) dropwise. The reaction mixture was stirred at 0° C. for one h. The reaction was quenched with water (1 mL) and 1N NaOH (2 mL) was added, forming a white slurry. The aqueous layer with extracted with EtOAc (2×10 mL) and the organic layers combined, washed with brine, dried with Na2SO4, filtered, and concentrated to yield a clear oil. 1H NMR (CD3OD, 400 MHz) δ (ppm): 3.38 (d, J=6.4 Hz, 2H), 2.05-1.97 (m, 2H), 1.83-1.64 (m, 4H), 1.58-1.50 (m, 1H), 1.29-1.19 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08211894B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-6d969926fe2a46fba87de71a13f1cf2d |
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| Source note | uspto-grants-2012_07 |
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