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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51306Generated: October 25, 2026

Chlorotrimethylsilane → Ethyl 3-cyclohexyl-3-methylbutanoate

https://huagongshe.com/reaction/51306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantEthyl 3,3-dimethylacrylateHCID 12516—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178478990HCID 178478990—
CatalystCuprous chlorideHCID 62652—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-cyclohexyl-3-methylbutanoateHCID 22289815—

Reaction Steps

Trimethylsilyl chloride (1.3 ml, 10.2 mmol), copper (I) chloride (30 mg, 0.3 mmol) and cyclohexylmagnesium chloride (4.6 ml, 2N in diethyl ether, 9.2 mmol) were added slowly to an ice-cooled solution of ethyl 3,3-dimethylacrylate (1 g, 8.5 mmol) in tetrahydrofuran (10 ml). The solution was stirred for 10 minutes, then allowed to warm to room temperature and stirred for an hour. Saturated aqueous ammonium chloride solution (10 ml) was added and the mixture was partitioned between water (10 ml) and diethyl ether (20 ml). The layers were separated and the aqueous phase was extracted with diethyl ether (2×10 ml). The combined organic extracts were dried (MgSO4) and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel using ethyl acetate:pentane(5:95) as eluant to afford the title compound, 1.2 g. 1H-NMR (CDCl3, 400 MHz) δ: 0.75 (m, 8H), 1.05-1.28 (m, 7H), 1.62 (m, 1H), 1.78 (m, 4H), 2.20 (s, 2H), 4.10 (q, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713496B2
Source datasetuspto-grants-2004_03
ORD IDord-34c3090648704563a602edad49707405
Source noteuspto-grants-2004_03