HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 2-Propen-1-one,1-(5-methyl-2-thienyl)-3-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Acetyl-5-methylthiophene | HCID 83655 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Propen-1-one,1-(5-methyl-2-thienyl)-3-phenyl- | HCID 238607 | 67.2% |
Reaction Steps
A stirred solution of 2.2 grams (0.055 mole) of sodium hydroxide in 20 ml of ethanol was cooled to 0° C. and a mixture of 4.0 grams (0.03 mole) of 2-acetyl-5-methylthiophene and 3.1 grams (0.03 mole) of benzaldehyde in 5 ml of ethanol was added dropwise. Upon completion of addition the reaction mixture was allowed to warm to ambient temperature where it stirred for 16 hours. The reaction mixture was poured into aqueous 1N hydrochloric acid and extracted with methylene chloride. The extract was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to yield 4.6 grams of 1-(5-methyl-2-thienyl)-3-phenyl-2-propen-1-one as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04939165 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-70d25324e4b141e2a8305046095b2240 |
| Source note | uspto-grants-1990_07 |