HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2,2-Diethoxyethyl)dimethylamine → HCID 131711015, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2,2-Diethoxyethyl)dimethylamine | HCID 77163 | — |
| Reactant | 2-Chloro-1-[5-(4-nitrophenyl)furan-2-yl]ethan-1-one | HCID 21389361 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131711015 | HCID 131711015 | 86% |
Reaction Steps
Dimethylaminoacetaldehyde diethyl acetal (29 g, 0.18 mole) was added dropwise to a stirred mixture of 40 g (0.15 mole) of chloromethyl 5-(4-nitrophenyl)-2-furyl ketone in 750 ml of absolute ethanol at 30° over 15 minutes. The mixture was heated under reflux for 22 hrs and was filtered hot to remove a black insoluble material. The filtrate was cooled in ice, and the brown solid was filtered and discarded. The filtrate was diluted with 1.5 liters of anhydrous ether, and the solid which was deposited was collected by filtration to give 45 g (69%) of (2,2-diethoxyethyl)dimethyl[5-(4-nitrophenyl)-2-furoylmethyl] ammonium chloride hemihydrate. Two recrystallizations from CH3CN gave an analytical sample, m.p. 113°-118°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04066671 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-3f0a2f3dd4d74a18ab0a46df57df333f |
| Source note | uspto-grants-1978_01 |