HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 6-Dibenzylamino-benzo[b]thiophene-2-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 6-aminobenzo[b]thiophene-2-carboxylate | HCID 15557582 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Dibenzylamino-benzo[b]thiophene-2-carboxylic acid methyl ester | HCID 58969063 | — |
Reaction Steps
Methyl 6-aminobenzothiophene-2-carboxylate (29 mg, 0.140 mmol) was dissolved in 1 mL of anhydrous DMF and reacted with benzyl bromide (40 μL, 0.38 mmol) in the presence of potassium carbonate (41 mg, 0.30 mmol) at 80° C. under a nitrogen atmosphere for 16 h. The reaction mixture was used in the next step without further purification. MS (EI): cal'd 388 (MH+), exp 388 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935724B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-8995d6cc590c4da5ae172e52abf823aa |
| Source note | uspto-grants-2011_05 |