HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl methoxyacetate → HCID 54243492, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl methoxyacetate | HCID 80507 | — |
| Reactant | HCID 178478127 | HCID 178478127 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54243492 | HCID 54243492 | — |
Reaction Steps
A solution of 1,1-bis(3-chlorophenyl)-2-methoxyethanol (47 g) (obtained by the reaction of 3-chlorophenylmagnesium bromide with methyl 2-methoxyacetate in THF) in formic acid (44 cc) is heated to reflux for 5 hours, cooled and poured into a mixture of saturated sodium carbonate solution (500 cc) and ethyl acetate (300 cc). The organic phase is washed with water (3×250 cc) and with saturated sodium chloride solution (200 cc), then dried and concentrated to dryness under reduced pressure (2.7 kPa) to give bis(3-chlorophenyl)acetaldehyde (36.9 g) in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112988 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-c8ab7622acdf431189ad16ee7b21d7e2 |
| Source note | uspto-grants-1992_05 |