HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → HCID 86762097, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | HCID 66680630 | HCID 66680630 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86762097 | HCID 86762097 | — |
Reaction Steps
A mixture of N-((R)-5-bromoindan-2-yl)-4-cyclopropylmethoxybenzamide (6.70 g) and THF (67 ml) was cooled to −78° C. (dry ice bath), and a solution of methyllithium (7.5 ml; 3 M) was added dropwise. One minute after the addition had ended, a solution of butyllithium (10 ml; 2.5 M in toluene) was added dropwise. One minute after the addition had ended, DMF (3.8 g) and, after a further 30 seconds, acetic acid (1.5 ml) were added. After warming to room temperature, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic phases were dried over magnesium sulfate and concentrated. This afforded the product with the molecular weight of 335.41 (C21H21NO3); MS (ESI): 336 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552199B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-7b3e93ae3f91442280c6086a4d1b962b |
| Source note | uspto-grants-2013_10 |