Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-bromo-2,3-dihydro-1H-indene | HCID 10965463 | — |
| Reactant | HCID 54475451 | HCID 54475451 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20188223 | HCID 20188223 | — |
Reaction Steps
0.73 g of magnesium turnings are covered with 90 ml of dry diethylether. To that mixture is then added 6 g of 2-bromoindane in 20 ml of dry diethylether at such a rate that a gentle boiling is maintained. When the magnesium turnings have reacted the solution containing the Grignard reagent is cooled to room temperature. The reaction mixture is then added dropwise, over a period of 3 hours, to a cooled (0°-5° C. solution of diethoxyacetic acid piperidinyl amide (6.4 g) in 20 ml of dry diethylether. After the addition is complete, the reaction mixture is stirred for two hours at about 5° C. The mixture is then poured into a cold 2% sulfuric acid solution (50 ml). The solution is extracted with ether and the combined ether extracts are washed with water and evaporated to dryness to give a residue of crude product, which is used without purification in step (b).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04689339 |
|---|
| Source dataset | uspto-grants-1987_08 |
|---|
| ORD ID | ord-e661ba1483df42c9a16946f9259de1b6 |
|---|
| Source note | uspto-grants-1987_08 |
|---|