HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bicarbonate Ion → 1-Bromo-4-(dimethoxymethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 1-Bromo-4-(dimethoxymethyl)benzene | HCID 688342 | — |
Reaction Steps
50 g of 4-bromobenzaldehyde and 30 ml of o-triethyl formate are agitated for 5 hours at room temperature in 60 ml of methanol and 0.8 ml of thionyl chloride. After that, another 0.2 ml of thionyl chloride are added. The batch is poured into aqueous bicarbonate solution after 30 minutes and extracted with chloroform, washed with aqueous bicarbonate solution and water, dried above sodium sulfate, and concentrated by evaporation under reduced pressure. 68 g of 4-bromobenzaldehyde dimethyl ketal are obtained in the form of colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05693628 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-57cd6d343b11454cb3a908a663b7c964 |
| Source note | uspto-grants-1997_12 |