HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558162Generated: October 29, 2026
(Trifluoromethyl)trimethylsilane → HCID 66999612, compound
https://huagongshe.com/reaction/558162
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Reactant | HCID 87231630 | HCID 87231630 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66999612 | HCID 66999612 | 91% |
Reaction Steps
Add tetrabutylammonium triphenyldifluorosilicate (29.8 g, 55.19 mmol) to a stirring mixture of (S,E)-N-(1-(2-bromo-4-fluorophenyl)ethylidene)-2-methylpropane-2-sulfinamide (13 g, 42.46 mmol) in THF. Cool the mixture to about −60° C. and add the (trifluoromethyl)trimethylsilane over about 10 min. Warm up to −55° C. and stir for 2 h. Continue to warm up to 0° C. Cool the mixture back to −30° C., and quench with saturated NH4Cl (150 mL). Extract product into ethyl acetate (2×200 mL). Combine extracts, wash with aqueous saturated sodium chloride, dry over Na2SO4, filter, and concentrate. Purify the material on 700 g silica eluting with 8:2 to 1:1 hexanes:ethyl acetate to a crude material. Crystallize the material to give long needles (9.7 g, 91%). MS (ES) m/z 377 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063035B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-3e424ed68af74ec0856fe09ba9d8a77b |
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| Source note | uspto-grants-2011_11 |
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