Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631432Generated: November 4, 2026

Triethylsilane → HCID 178515018, compound

https://huagongshe.com/reaction/1631432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantCyclopropanecarboxaldehydeHCID 123114—
ReactantHCID 178455354HCID 178455354—
Catalystbismuth(III) bromideHCID 82232—
SolventAcetonitrileHCID 6342—
ProductHCID 178515018HCID 178515018100.9%

Reaction Steps

A stirred solution of 12B (750 mg, 2.086 mmol) in acetonitrile (10 mL) was treated with triethylsilane (0.432 mL, 2.71 mmol) and tribromobismuthine (94 mg, 0.209 mmol), followed by slow addition of cyclopropanecarbaldehyde (175 mg, 2.503 mmol) (dissolved in acetonitrile (0.5 mL)). The reaction mixture was stirred at room temperature overnight. The dark solid was removed by filtration, the filtrate was concentrated, and the residue was purified by ISCO silica column (24 g), gradient elution with ethyl acetate:hexane (0%-100% ethyl acetate over 15 min). Concentration of the desired fractions yielded 12C (630 mg, 2.104 mmol, >quantitative yield) as a white solid. MS (ES): m/z=322 [M+Na]+. 1H NMR (400 MHz, CDCl3) δ ppm 7.56-7.65 (m, 2H); 7.46-7.53 (m, 2H); 3.89-3.99 (m, 1H); 3.13-3.22 (m, 1H); 3.12 (d, 2H, J=6.8 Hz); 2.04-2.16 (m, 2H); 1.92-2.00 (m, 2H); 1.52-1.61 (m, 2H); 1.14-1.27 (m, 2H); 0.80-0.92 (m, 1H); 0.30-0.39 (m, 2H); −0.02-0.05 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791257B2
Source datasetuspto-grants-2014_07
ORD IDord-5148fdb928f8419db5a93b8621ebbe63
Source noteuspto-grants-2014_07