HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269265Generated: October 31, 2026
Tetrahydrofuran → 4-(1,1-Dimethyl-4,4,4-trifluoro-2-butynyl)anisole
https://huagongshe.com/reaction/2269265
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 5-(Trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate | HCID 2777507 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 4-(1,1-Dimethyl-4,4,4-trifluoro-2-butynyl)anisole | HCID 18677590 | 13% |
Reaction Steps
To a stirred solution of Compound 56 (0.22 g, 1.26 mmol) in THF (8 ml) was added n-BuLi (1.69 M in hexane, 0.82 ml, 1.39 mmol) at −78° C. under N2, then warmed up to 0° C., and stirred for 1 h. S-(Trifluoromethyl)dibenzothiophenium trifluoromethane-sulfonate (1.01 g, 2.52 mmol) was added, and stirred for 3 h at 0° C. The mixture was quenched by the addition of NaHCO3 aq., and extracted with CH2Cl2. The combined organic layers were dried over MgSO4, filtered, and concentrated. This was purified by SiO2 chromatography to give Compound 57 (38 mg, 13%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329396B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-65b09b873966426fb341b59ac38de3fc |
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| Source note | uspto-grants-2001_12 |
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