Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (-)-Isopulegol | HCID 170833 | — |
| Solvent | Water | HCID 962 | — |
| Product | (+)-Isopulegol | HCID 1268090 | — |
Reaction Steps
After the catalyst solution obtained in Example 34-1 was cooled to from 0 to 5° C., 1.54 g (10.0 mmol, optical purity: 96.6% e.e.) of 1-citronellal ((S)-citronellal) was added dropwise. The resulting mixture was stirred overnight at from 0 to 5° C. After completion of the reaction, 2 mL of water was added to the reaction mixture. The organic layer was analyzed using gas chromatography. As a result, it was found that a substrate conversion ratio was 89.2%, an isopulegol selectivity was 88.1%, and a d-n-isopulegol:(the other isomers) ratio was 96.9:3.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09061959B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-79d33d735fd84177a5a8c7f08540813f |
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| Source note | uspto-grants-2015_06 |
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