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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015379Generated: November 2, 2026

Triethylsilane → HCID 67301354, compound

https://huagongshe.com/reaction/1015379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantHCID 67302137HCID 67302137—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 67301354HCID 6730135491.2%

Reaction Steps

In a 100 mL flask with stir bar and 4-(2-methoxybenzoyl)cyclohexanecarboxylic acid methyl ester (900 mg; 3.26 mmol), trifluoroacetic acid (10 mL) was chilled to 0° C. and triethylsilane (2 g; 16.3 mmol) was added over 1 minute. Mixture was allowed to warm to room temperature. After 48 hours, mixture was concentrated in vacuo and reduced by half volume. The mixture was poured into a water (40 mL) solution and extracted with ethyl acetate (EtOAc) (4×10 mL). The combined organic layers were washed with NaHCO3 (40 mL), brine (40 mL) and dried over anhydrous Na2SO4. The organic layer was concentrated in vacuo to obtain the crude mixture, which was purified by of silica gel flash chromatography, using EtOAc/hexane (gradient system), to obtain 4-(2-methoxybenzyl)cyclohexanecarboxylic acid methyl ester (0.78 g, 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985755B2
Source datasetuspto-grants-2011_07
ORD IDord-784647dfb97342cd95f46f8aaa747698
Source noteuspto-grants-2011_07