HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 54162423, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 54202865 | HCID 54202865 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 54162423 | HCID 54162423 | 94.8% |
Reaction Steps
A solution of 1,1-bis-(3-tolyl)-2-methoxyethanol (24.66 g) (obtained by reaction of (3-tolyl)magnesium bromide on methyl 2-methoxyacetate in tetrahydrofuran) in formic acid (30 cc) is refluxed for 12 hours, cooled and poured into a mixture of saturated sodium carbonate solution (400 cc) and ethyl acetate (400 cc). The organic phase is washed with water (3×300 cc) and with saturated sodium chloride solution (300 cc), then dried and concentrated to dryness under reduced pressure (2.7 kPa) to give bis-(3-tolyl)acetaldehyde (20.45 g) in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05102667 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-91ca2a935cc84ade861b51c7fe7099a2 |
| Source note | uspto-grants-1992_04 |