Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Carbonate | HCID 11125 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | HCID 21196037 | HCID 21196037 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21196126 | HCID 21196126 | — |
Reaction Steps
Under a nitrogen atmosphere bromoacetylbromide (1.31 ml, 0.015 mol) was added to a slurry of 2-[4-chlorophenoxymethyl]-1H-indole (0.81 g, 0.003 mol), and lithium carbonate (2.22 g, 0.03 mol) in diethyl ether (37.5 ml). The resulting mixture was heated to 55° C. The progress of the reaction was monitored by thin layer chromatography. The reaction mixture was partitioned between diethyl ether and a sodium bicarbonate solution. The organic fraction was washed with water and then brine, and then dried over sodium sulfate. The solvents were removed in vacuo. Yield: 1.34 g. NMR was consistent with the proposed title structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06245761B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-67ae0ecfb3b74363ba4ddab8616fd771 |
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| Source note | uspto-grants-2001_06 |
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