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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868144Generated: November 2, 2026

(Trifluoromethyl)trimethylsilane → HCID 68551826, compound

https://huagongshe.com/reaction/1868144

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 68554748HCID 68554748—
ProductHCID 68551826HCID 6855182681%

Reaction Steps

To a solution of (R)-1-(4-(4-(2,4-difluorophenyl)-2-methylpiperazin-1-ylsulfonyl)phenyl)ethanone (360 mg, 0.87 mmol, prepared according to procedures similar to those described in Example 29A) was added TMSCF3 (5.2 mL, 0.5 M in THF, 2.6 mmol) and TBAF (0.87 mL, 1 M in THF, 1.0 mmol) at 0° C. The resultant mixture was stirred for 6 h then rt overnight. It washed with aq. NH4Cl and aq. layer was extracted with DCM. The organic layer was dried over Na2SO4. The crude product was purified on SiO2 column eluted with hexanes/EtOAc to give the desired product as a white solid (329 mg, 81%). HRMS: calcd for C20H21F5N2O3S+H+, 465.12658. found (ESI-FTMS, [M+H]1+), 465.12565.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632838B2
Source datasetuspto-grants-2009_12
ORD IDord-c21c5e0479f742f0bd15f74c3c270717
Source noteuspto-grants-2009_12