HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430018Generated: October 26, 2026
Sulfuric Acid → (S)-2-Methoxycyclohexanone
https://huagongshe.com/reaction/430018
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methoxycyclohexanol | HCID 19938756 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Product | (S)-2-Methoxycyclohexanone | HCID 642158 | — |
Reaction Steps
Reaction was carried out in the same manner as in Example 16. After the peak due to (S)-2)-methoxycyclohexanol had disappeared, the reaction solution was given 2 g of sodium hydrogensulfite with stirring so that the reaction solution did not change potassium iodide starch paper into purple any longer. The reaction solution was adjusted to pH 2 or below with 10% sulfuric acid, followed by stirring at 20-25° C. for 1 hour. The reaction solution was adjusted to pH 7.5-8 with an aqueous solution of sodium carbonate, followed by stirring at 20-25° C. for 1 hour. The reaction solution was adjusted again to pH 2 or below with 10% sulfuric acid, followed by stirring at 20-25° C. for 2 hours. The reaction solution was extracted three times with 100 g of toluene. The toluene layers were combined together and washed with a saturated aqueous solution of sodium chloride. After concentration and distillation in the same manner as in Example 1, there was obtained 10.3 g (80 mmol) of (S)-2-methoxycyclohexanone having a chemical purity of 99.3% and an optical purity of 99.6% ee. This product was heated at 60° C. for 48 hours in the same manner as in Example 16; it decreased in optical purity to 99.0% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06320069B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-148a497e61574ab39fb3935ab3ac4104 |
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| Source note | uspto-grants-2001_11 |
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