Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | 6-Ethoxy-2,3-dihydro-1H-inden-1-one | HCID 15039152 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 73991630 | HCID 73991630 | — |
Reaction Steps
A solution of 6-ethoxy-1-indanone and isoamylnitrite (1.5 eq.) in ethyl acetate arecooled to approximately 0° C. and concentrated hydrochloric acid (1.1 acid equivalents) is added at a rate to keep the temperature below 40° C. After the addition is completed the slurry is stirred at 5-10° C. until analysis indicated that all of the starting material is consumed. The product is filtered and rinsed with cold ethyl acetate. The oxime product (5) can be easily purified by refluxing as a slurry in anhydrous ethanol, cooling filtering, and then washing the solid with more ethanol and then drying (m.p. 220° C. decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06410787B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-1c27a6d95735431b820e44a6e93949a4 |
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| Source note | uspto-grants-2002_06 |
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