HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminophenol → N-(2-Hydroxyphenyl)prop-2-enamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N-(2-Hydroxyphenyl)prop-2-enamide | HCID 12998435 | — |
Reaction Steps
Among the (meth)acrylamide derivatives represented by the general formula (1), a compound (the above compound A-1) in which R1 is a hydrogen atom; R2 is an ethoxymethyl group; and R3 to R6 are a hydrogen atom can be synthesized, for example, by the following manner. In this manner, o-aminophenol is reacted with acryloyl chloride in N-methyl-2-pyrrolidone (NMP) in the presence of lithium chloride to obtain N-(2-hydroxyphenyl)acrylamide. N-(2-hydroxyphenyl)acrylamide is then reacted with chloromethyl ethyl ether in NMP in the presence of N,N-diisopropyl ethylamine to synthesize the above compound A-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939241B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-d4e903e85a594f5b8fefebb323e0f11b |
| Source note | uspto-grants-2011_05 |