HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 6-((2-Ethylhexyl)(phenyl)amino)hexyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | 6-((2-Ethylhexyl)(phenyl)amino)hexan-1-ol | HCID 67046281 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-((2-Ethylhexyl)(phenyl)amino)hexyl acetate | HCID 57857729 | 93.8% |
Reaction Steps
6-((2-ethylhexyl)(phenyl)amino)hexan-1-ol (8.0 g, 0.023 mol) and dichloromethane (100 ml) were loaded into a three-neck flask, stirred, and added with acetic anhydride (2.8 g, 0.028 mol) and pyridine (3.0 g, 0.038 mol). The mixture was allowed to react at 40° C. for 12 hours with stirring. The reaction product was transferred into a separate funnel, and was then added with water and dichloromethane, after which the organic layer was isolated therefrom, dehydrated using sodium sulfate, and then distilled under reduced pressure. Subsequently, the obtained viscous liquid was separated through silica column chromatography, thus obtaining 7.5 g of a yellowish transparent liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915428B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-f3b9171a85224812a8fd2acec1063b2c |
| Source note | uspto-grants-2011_03 |