HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-[1-m-Tolyl-meth-(e)-ylidene]-succinic acid diethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | 3-Methylbenzaldehyde | HCID 12105 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Product | 2-[1-m-Tolyl-meth-(e)-ylidene]-succinic acid diethyl ester | HCID 68599965 | — |
Reaction Steps
To a solution of 22.6 g sodium ethylate in 440 ml of ethanol, 20 g of 3-Methyl-benzaldehyde and 31 g of Malonic acid diethyl ester dissolved in 100 ml ethanol was added drop-wise over 1.5 h at 50° C. Then, the reaction mixture was heated to reflux for 12 h. After cooling to RT half of the solvent was evaporated under reduced pressure and diluted with 200 ml of water. The remaining reaction mixture was acidified to pH 1 by addition of concentrated hydrochloric acid and then extracted with ethyl acetate. The organic phase was dried over MgSO4 and the solvents were removed under reduced pressure. The crude product was pure enough for the next reaction step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08669266B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-856b0933d5a644fb8a7417c8e1615e3f |
| Source note | uspto-grants-2014_03 |