Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 18609506 | HCID 18609506 | — |
| Reactant | HCID 20188225 | HCID 20188225 | — |
| Reactant | HCID 54146119 | HCID 54146119 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15338831 | HCID 15338831 | — |
Reaction Steps
Bromine in methylene chloride is slowly added to a stirred solution of cis-1-(2,3-dihydro-1-methyl-1H-inden-2-yl)ethanone (34.8 g) in methylene chloride (835 ml), while keeping the temperature at +10° C. The reaction is followed by GLC. The first products are the isomers of 1-(2-bromo-2,3-dihydro-1-methyl-1H-inden-2-yl)ethanone and cis-2-bromo-1-(2,3-dihydro-1-methyl-1H-inden-2-yl)ethanone. When the added amount of bromine is about 0.3 mol, only the final product, 2-bromo-1-(2-bromo-2,3-dihydrol-methyl-1H-inden-2-yl)ethanone is visible in the chromatogram and the mono bromo products cannot be seen in the chromatogram any more. The methylene chloride solution is washed with water, then several times with the diluted NaHCO3 solution and finally with water. The solvent is dried with Na2SO4 and evaporated to dryness.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04689339 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-8626b45b275c4e28bae2be02833668e2 |
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| Source note | uspto-grants-1987_08 |
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