HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 15678802, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-[(4-Chlorophenyl)methyl]-5-hydroxy-3-methyl-1H-indole-2-propanoic acid | HCID 15678782 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15678802 | HCID 15678802 | — |
Reaction Steps
Using 845 mg of the product of Example 23 as starting material, diluted in 23 ml of dimethyl ketone, 476 mg of potassium carbonate and 225 μl of allyl bromine was added. The reaction was refluxed overnight. The reaction was then diluted with water and the acetone removed in vacuo. Then the reaction was extracted with CH3CO2Et and the organic phase was dried and concentrated to yield after flash chromatography (hexane 8, ethyl acetate 2) 790 mg of the compound, which was then hydrolyzed following the procedure of Example 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05081145 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-923aaa4b0f2c45738394d853fb25f016 |
| Source note | uspto-grants-1992_01 |