HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Hex-3-en-3-yl-1,3,2-benzodioxaborole → 2-[2-(-1-Ethyl-but-1-enyl)-3-methyl-benzoylamino]-indan-2-carboxylic acid ethyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Hex-3-en-3-yl-1,3,2-benzodioxaborole | HCID 5046852 | — |
| Edukt | 2-(2-Iodo-3-methyl-benzoylamino)-indan-2-carboxylic acid ethyl ester | HCID 59314153 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 2-[2-(-1-Ethyl-but-1-enyl)-3-methyl-benzoylamino]-indan-2-carboxylic acid ethyl ester | HCID 68591165 | 146,8% |
Reaktionsschritte
To a solution of 2-(2-iodo-3-methyl-benzoylamino)-indan-2-carboxylic acid ethyl ester (400 mg, 0.89 mmol) and 2-(1-Ethyl-but-1-enyl)-benzo[1,3,2]dioxaborole (709 μL, 3.56 mmol) in dioxane (15 mL) is added Pd(PPh3)4 (103 mg, 8.9% mmol) and 2M aqueous solution of CsCO3 (1.34 mL, 2.67 mmol). The resulting reaction mixture is covered with argon and run in a microwave reaction: 110° C., 2 h. After concentration in vacuo, the residue is purified by flash column chromatography (120 g silica gel, gradient elution: 5%-50% EtOAc in heptane) to give a pure product (128) as a brown semi-solid (530 mg, 73%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08569535B2 |
| Quelldatensatz | uspto-grants-2013_10 |
| ORD ID | ord-b3dfef23d1ea4d1f962aa1af8830ce7d |
| Quellennotiz | uspto-grants-2013_10 |