HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cinnamaldehyde → HCID 10456106, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cinnamaldehyde | HCID 637511 | — |
| Reactant | HCID 86605018 | HCID 86605018 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10456106 | HCID 10456106 | 95% |
Reaction Steps
1-(2-Chloropyridin-4-yl)carbonylspiro[indoline-3,4′-piperidine]trifluoroacetic acid salt (0.44 g) and trans-cinnamaldehyde (0.29 g) were suspended in tetrahydrofuran (8 ml) and ethanol (6 ml). Borane-pyridine complex (0.26 ml) was added and the reaction stirred vigorously overnight at room temperature. The mixture was evaporated and partitioned between dichloromethane and water. The organics were dried over anhydrous magnesium sulfate and evaporated in vacuo. Flash chromatography [SiO2; ethyl acetate-hexane-triethylamine (25:75:1), increasing polarity to (50:50:1)] yielded 0.42 g (94%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174987B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-6b2c3c616d5046d88dac6a5f436f22f1 |
| Source note | uspto-grants-2015_11 |