HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 14329997, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(5-Chloro-2,4-dihydroxy-3-propylphenyl)ethan-1-one | HCID 13389172 | — |
| Reactant | HCID 70419125 | HCID 70419125 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14329997 | HCID 14329997 | 38% |
Reaction Steps
A mixture of 0.990 g (0.0043 mole) of 1-(5-chloro-2,4-dihydroxy-3-propylphenyl)ethanone, 1.980 g (0.0043 mole) of 4-[4-acetyl-3-[(5-bromopentyl)oxy]-3-propylphenoxy]butanoic acid ethyl ester and 1.2 g (0.0087 mole) of anhydrous potassium carbonate in 40 ml of anhydrous acetone and 20 ml of anhydrous dimethylformamide was stirred at reflux for 22 hours. The reaction mixture was concentrated in vacuo and the residue was purified by HPLC using 25% ethyl acetate-hexane to give 1.008 g (38% yield) of 4-[4-acetyl-3-[5-(4-acetyl-6-chloro-3-hydroxy-2-propylphenoxy)pentyloxy]-2-propylphenoxy]butanoic acid ethyl ester as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04507498 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-9df86de3caac46fca70e989b601ab1d1 |
| Source note | uspto-grants-1985_03 |