HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291825Generated: October 31, 2026
Dimethylformamide dimethyl acetal → HCID 54308355, compound
https://huagongshe.com/reaction/1291825
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | HCID 18918264 | HCID 18918264 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54308355 | HCID 54308355 | — |
Reaction Steps
To a solution of the product of step (i) (10 g) in dry DMF (80 ml) was added dimethylformamide dimethyl acetal (DMFDMA) (30 ml) and the reaction mixture was heated to reflux. After 2 days a further quantity of DMFDMA (30 ml) was added and refluxing was continued for a further 2 days. The reaction mixture was evaporated and the residue partitioned between aqueous ammonium chloride solution and ethyl acetate. The organic layer was separated, washed with brine, dried (MgSO4) and evaporated. The residue was purified by flash chromatography on silica by elution with ethyl acetate to yield 1-ethoxycarbonyl-4-(1-dimethylamino-2-methoxycarbonylethen-2-yl)-piperazine (7 g) as an orange oil: NMR (CDCl3) δ 1.28 (3H, t), 2.90 (4H, m), 3.14 (6H, s), 3.50 (4H, m), 3.64 (3H, s), 4.12 (2H, q), 7.01 (1H, s); m/Z 286 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05753659 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-7fefd102ecaa4997a20239909e30170a |
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| Source note | uspto-grants-1998_05 |
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