HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51306Generated: October 25, 2026
Chlorotrimethylsilane → Ethyl 3-cyclohexyl-3-methylbutanoate
https://huagongshe.com/reaction/51306
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Ethyl 3,3-dimethylacrylate | HCID 12516 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178478990 | HCID 178478990 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-cyclohexyl-3-methylbutanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713496B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-34c3090648704563a602edad49707405 |
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| Source note | uspto-grants-2004_03 |
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