HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 86701139, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-(Methylamino)ethanol | HCID 8016 | — |
| Reactant | HCID 86701140 | HCID 86701140 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86701139 | HCID 86701139 | 56% |
Reaction Steps
A solution of paraformaldehyde (0.122 g), 2-(methylamino)ethanol (0.330 g), and acetic acid (0.13 ml) in ethanol (4 ml) was stirred at 80° C. for 2 hours. After cooling, a solution of compound (6) (0.200 g) in methylene chloride (4 ml) was added to the reaction solution, and the mixture was stirred overnight at room temperature. The reaction solution was partitioned between chloroform and water. The organic layer was neutralized with an aqueous sodium bicarbonate solution, then washed with brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was then purified by neutral silica gel column chromatography (chloroform/methanol) to obtain compound (37) (0.130 g, 56%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912181B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-4e194103f44b40f6869a72eda34b93ee |
| Source note | uspto-grants-2014_12 |