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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211903Generated: October 31, 2026

Triethylsilane → HCID 21963517, compound

https://huagongshe.com/reaction/2211903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantHCID 13355716HCID 13355716—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 21963517HCID 2196351756.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

Triethylsilane (1.60 mL, 10.017 mmol) was added via syringe to a stirred solution of N-[4-{2-bromo-acetyl)-2-fluoro-phenyl]-acetamide (1.1435 g, 4.172 mmol) in trifluoroacetic acid (14.0 mL) under nitrogen. The reaction was heated on an oil bath to 60° C. After 2.5 h, the reaction mixture was poured into ice water and allowed to warm to rt. The crude product was extracted with methylene chloride (2×75 mL). The combined organic extracts were washed with brine (50 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The residue was crystallized from methanol and water to provide 0.6109 g (2.349 mmol) of the product as a white solid. Yield: 56%; MS (APCI): 260 [M+H]+, 262 [M+H+2]+; 1H NMR (400 MHz, CDCl3) δ 8.22 (dd, J=8.3, 8.5 Hz, 1H), 7.30 (br s, 1H), 6.93–6.97 (m, 2H), 3.51 (t, J=7.3 Hz, 2H), 3.10 (t, J=7.3 Hz, 2H), 2.20 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101886B2
Source datasetuspto-grants-2006_09
ORD IDord-3e609e55186c4c97810bca83251b5a47
Source noteuspto-grants-2006_09