HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718003Generated: October 29, 2026
(Methoxymethyl)trimethylsilane → HCID 86713710, compound
https://huagongshe.com/reaction/718003
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Methoxymethyl)trimethylsilane | HCID 139809 | — |
| Reactant | Cyclohexanone, 3-(4-chlorophenyl)- | HCID 11241243 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86713710 | HCID 86713710 | — |
Reaction Steps
To a solution of (methoxymethyl)trimethylsilane (694 mg, 5.75 mmol) in tetrahydrofuran (6.8 mL) at −78° C. was added drop-wise sec-butyllithium (1.4 M, 4.45 mL, 6.23 mmol). The solution was warmed to −25° C., held at that temperature for 30 minutes, then cooled to −78° C. To the reaction was added drop-wise 3-(4-chlorophenyl)cyclohexanone (prepared according to the method of G. A. Whitlock et al., Bioorg. Med. Chem. Lett. 2009, 19, 3118-3121) (1.0 g, 4.8 mmol). The reaction was warmed to −25° C. and stirred for 30 minutes, then allowed to slowly warm to room temperature and stir for 48 hours. The reaction was diluted with tetrahydrofuran (10 mL), quenched with saturated aqueous ammonium chloride solution, and extracted three times with ethyl acetate. The combined organic layers were dried over magnesium sulfate and concentrated in vacuo to provide the crude title compound as a pale yellow oil. Yield: 1.25 g. This material was used directly in the following step. GCMS m/z 236 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193726B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-7f9ff1d4a41f47da817915f01e454c90 |
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| Source note | uspto-grants-2015_11 |
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