HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 2-(2-Allyloxy-3-chloro-benzoylamino)-indan-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-(3-Chloro-2-hydroxy-benzoylamino)-indan-2-carboxylic acid ethyl ester | HCID 59314122 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Allyloxy-3-chloro-benzoylamino)-indan-2-carboxylic acid ethyl ester | HCID 59314268 | 58% |
Reaction Steps
To a suspension of 2-(3-chloro-2-hydroxy-benzoylamino)-indan-2-carboxylic acid ethyl ester (14) (250 mg, 0.69 mmol), anhydrous Cs2CO3 (453 mg, 1.39 mmol), and KI (23 mg, 0.14 mmol) in DMF (10 mL) is added 3-bromo-propene (70 μL, 0.83 mmol). The resulting reaction suspension is stirred at RT overnight. After the removal of DMF in vacuo, the residue is dissolved in EtOAc (20 mL) and washed with water (1×5 mL) and brine (2×5 mL). The organic layer is dried over anhydrous Na2SO4 and concentrated in vacuo. The residue is purified by flash column chromatography (80 g silica gel, gradient elution: 10-40% EtOAc in heptane) to give a pure product (17) as white solid (160 mg, 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569535B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-acfbf89732674dd9b1b54ac1895b9804 |
| Source note | uspto-grants-2013_10 |