HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 23131715, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl Thioglycolate | HCID 16907 | — |
| Reactant | 3-(Bromomethyl)benzaldehyde | HCID 7127825 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 23131715 | HCID 23131715 | — |
Reaction Steps
To a mixture of 1.00 g of 3-(bromomethyl)benzaldehyde and 20 ml of ethanol were added 0.65 ml of methyl thioglycolate and 0.47 g of potassium carbonate, and the mixture was stirred at room temperature for 2.5 hours. To the reaction mixture was added diethyl ether, this was washed with an aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to obtain 0.36 g of oily 3-[(methoxycarbonylmethylthio)methyl]benzaldehyde [Compound No. (u)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691883B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-a8d81abab54e4aef8b86f405905fb6ff |
| Source note | uspto-grants-2010_04 |