HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetamide, N-(3-methoxyphenyl)- → HCID 23312582, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetamide, N-(3-methoxyphenyl)- | HCID 11494 | — |
| Reactant | Valeryl chloride | HCID 61186 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23312582 | HCID 23312582 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
The mixture consisting of 49.5 g of N-acetyl-m-anisidine, 72.3 cc of valeric acid chloride and 200 cc of methylene chloride is cooled to 0° C. 120 g of aluminum chloride are added little by little. The reaction mixture is refluxed for 2 hours with stirring, cooled, then poured in ice water. The resulting oily product is extracted with chloroform. The chloroform phase in turn is extracted with 2N sodium hydroxide solution which is then acidified. Thus, 24 g of 5-acetamido-2-valeryl phenol (MP 113° C.) are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04600788 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-63d91d739a6e4d36b1d64925c4313567 |
| Source note | uspto-grants-1986_07 |