HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Ethyl cinnamoylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl cinnamoylacetate | HCID 54004396 | — |
Reaction Steps
A solution of 0.020 moles of titanium tetrachloride in 15 ml of carbon tetrachloride was added over a period of 10 minutes to a cold (5°) solution of 0.015 moles of ethyl acetoacetate and 0.015 moles of benzaldehyde in 60 ml of tetrahydrofuran. After the mixture was stirred for 1.5 hours, a solution of 0.060 mole of triethylamine in 15 ml of tetrahydrofuran was added dropwise. The reaction mixture was then stirred for 20 hours, after which the title compound was isolated by the extraction and chromatography methods described in Example 1. The material prepared by this procedure was identical to that prepared by the method of Example 1, as indicated by the reverse phase chromatographic method described in Example 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04761503 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-7d7bafc6893e4fa1b0645219b53a09c3 |
| Source note | uspto-grants-1988_08 |