HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 1-Phthalimido-2-[2-(5-dimethylaminomethyl-2-furyl)ethylthio]ethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | 2-[[2-(2-Furanyl)ethyl]thio]ethyl-1H-isoindole-1,3(2H)-dione | HCID 23452113 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Phthalimido-2-[2-(5-dimethylaminomethyl-2-furyl)ethylthio]ethane | HCID 23452176 | 72.3% |
Reaction Steps
2-[[2-(2-Furanyl)ethyl]thio]ethyl-1H-isoindole-1,3(2H)-dione (0.5 g), dimethylamine hydrochloride (0.27 g) and paraformaldehyde (0.102 g) were heated together under reflux in ethanol. After 5 hr further dimethylamine hydrochloride (0.27 g) and paraformaldehyde (0.102 g) were added and the heating continued for a further 16 hr. Solvent was removed, the residue basified and extracted with ethyl acetate to give an oil which after column chromatography (silica/methanol) gave 2-[2-[[2-[5-(dimethylamino)methyl-2-furanyl]ethyl]thio]ethyl]-1H-isoindole-1,3(2H)-dione as a pale oil (0.43 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04169855 |
| Source dataset | uspto-grants-1979_10 |
| ORD ID | ord-ec0aae6b403846a2a7882f9a985da654 |
| Source note | uspto-grants-1979_10 |