HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxyacetanilide → HCID 725681, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxyacetanilide | HCID 12124 | — |
| Reactant | N-[3-(prop-2-en-1-yloxy)phenyl]acetamide | HCID 258024 | — |
| Reactant | 1-(Chloromethyl)-3-(2-propen-1-yloxy)benzene | HCID 14169367 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 725681 | HCID 725681 | — |
Reaction Steps
A mixture of N-(3-allyloxyphenyl)acetamide (13.2 g) prepared by a similar method to that of Example 2, Footnote c (A), from N-(3-hydroxyphenyl)acetamide, in Ph2O (100 ml) was heated at 250° C. for 10 minutes, cooled and diluted with hexane (100 ml) to give crystals. The crystals were re-crystallised from ethyl acetate. The liquors were evaporated and dissolved in 0.2M aqueous NaOH, filtered though Celite, and acidified with 1M aqueous HCl solution to give N-(4-allyl-3- hydroxyphenyl)acetamide (3.6 g) mpt. 164°-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811459 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-79c6bde1473548689f8d46caafbc8181 |
| Source note | uspto-grants-1998_09 |