HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indole → methyl trans-3-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indole | HCID 736229 | — |
| Reactant | Methyl 3-methoxyacrylate | HCID 5323651 | — |
| Reactant | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | methyl trans-3-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]acrylate | HCID 11221407 | 8.9% |
Reaction Steps
1.27 g of 3-(4-fluorophenyl)-1-isopropyl-1H-indole, 1.16 g of methyl trans-3-methoxyacrylate and 12 mL of glacial acetic acid were mixed, then, 797 mg of 30 wt % hydrogen bromide/acetic acid solution was added dropwise into the mixture at an inner temperature of 25° C., the mixture was stirred for 5 hours at the same temperature to cause a reaction. After completion of the reaction, the same post treatment was conducted as in Example 1 to obtain 0.15 g of methyl trans-3-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]acrylate (yellow solid). Yield: 8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700642B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-9b60ea2565b24b14a14ac677ad3b821f |
| Source note | uspto-grants-2010_04 |