HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059285Generated: October 31, 2026
Potassium Carbonate → HCID 18670412, compound
https://huagongshe.com/reaction/1059285
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (Methoxymethyl)trimethylsilane | HCID 139809 | — |
| Reactant | HCID 18670115 | HCID 18670115 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 18670412 | HCID 18670412 | — |
Reaction Steps
100 ml of a solution of 20.5 ml of (methoxymethyl)trimethylsilane in dry tetrahydrofuran was cooled under a nitrogen atmosphere. Then 92 ml of a 1.3 M solution of s-butyllithium in cyclohexane was added dropwise thereinto at −78° C. After the completion of the addition, the mixture was stirred at −35° C. for 30 minutes. After adding 10.9 g of 1,3,5-trimethyl-3-azabicyclo[3.3.1]nonan-9-one, the resulting mixture was stirred at room temperature for 2 hours and then poured into a cooled aqueous solution of ammonium chloride. Then it was made alkaline by adding potassium carbonate and extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous sodium sulfate. After distilling off the solvent under reduced pressure, 9.2 g of the title compound was obtained as a pale-brown oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518423B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-0f436956cea34f95af81e319ef9e143f |
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| Source note | uspto-grants-2003_02 |
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