HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 4-Benzoyloxy-2-methylenebutanal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 4-Oxobutyl benzoate | HCID 11008752 | — |
| Reactant | Dimethylazanium;chloride | HCID 12954980 | — |
| Product | 4-Benzoyloxy-2-methylenebutanal | HCID 18991529 | — |
Reaction Steps
10 g (52 mmol) of 4-benzoyloxybutanal, 4.78 g (58.6 mmol) of dimethylammonium chloride and 4.6 ml (60.8 mmol) of formaldehyde solution (37%) are refluxed for one hour with stirring (bath temperature ~110° C.). The mixture is allowed to cool and is extracted three times with ether; the organic phases are combined, washed with saturated sodium chloride solution, dried over MgSO4, filtered and concentrated by evaporation. 4-benzoyloxy-2-methylenebutanal is obtained in the form of a yellowish oil which can be reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05294734 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-75915d019b444692b1cbc9f1df203d57 |
| Source note | uspto-grants-1994_03 |