HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Butanal, 4-(acetyloxy)-2-methylene-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 4-Acetoxybutyraldehyde | HCID 11007927 | — |
| Reactant | Dimethylazanium;chloride | HCID 12954980 | — |
| Product | Butanal, 4-(acetyloxy)-2-methylene- | HCID 11083989 | — |
Reaction Steps
13.0 g (100 mmol) of acetic acid (4-oxo)butyl ester, 92.0 g (112.6 mmol) of dimethylammonium chloride and 10.8 ml (117 mmol) of 37% formaldehyde solution are heated at 100° for one hour with stirring. The mixture is allowed to cool and is extracted 3 times with 30 ml of diethyl ether each time. The organic phases are combined, washed with saturated sodium chloride solution, dried over magnesium sulfate and concentrated to dryness by evaporation. Acetic acid (3-formyl)but-3-enyl ester is obtained in the form of a colourless oil which can be reacted further without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05294734 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-b41997f41ab84659b2094cbaf5c18f5f |
| Source note | uspto-grants-1994_03 |