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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038214Generated: November 3, 2026

(Trifluoromethyl)trimethylsilane → HCID 86691229, compound

https://huagongshe.com/reaction/2038214

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantHCID 89713970HCID 89713970—
CatalystTetrabutylammonium AcetateHCID 82707—
SolventDimethylformamideHCID 6228—
ProductHCID 86691229HCID 8669122978%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

Add neat (trifluoromethyl)trimethylsilane (109 mL, 0.74 mol) at 0° C. to a stirred solution of tetrabutylammonium acetate (88 g, 0.29 mol) and (N—Z)—N-[(4-bromophenyl)methylene]-(R)-2-methyl-propane-2-sulfinamide (85 g, 0.29 mol) in DMF (1.2 L) at 0° C. Stir the mixture at 0-5° C. for 90 minutes. Add saturated aqueous ammonium chloride solution (1.2 L) and extract with EtOAc (4×400 mL). Combine the organic extracts and sequentially wash with water then brine (2×1 L); dry over magnesium sulphate; filter; and concentrate the filtrate under reduced pressure. Triturate the residue with hexane (200 mL) for 10 minutes; filter; and dry the filtrate under vacuum to afford the title compound as a yellow solid (81 g, 76% yield, >98 de). MS (m/z): 358 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575352B2
Source datasetuspto-grants-2013_11
ORD IDord-800e1343c4a04422b61ee434eeec3f0f
Source noteuspto-grants-2013_11