HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzo(B)Thiophene → Benzo(b)thiophene, 3-bromo-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzo(B)Thiophene | HCID 7221 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-[(Benzo[b]thiophene-3-yl)carbonyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester | HCID 15337456 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Benzo(b)thiophene, 3-bromo- | HCID 123250 | 48% |
Reaction Steps
4-[(Benzo[b]thiophene-3-yl)carbonyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester ##STR13## Dissolve benzo[b]thiophene (23 g, 0.170 mmol) in carbon tetrachloride (80 mL). Add, by dropwise addition, a solution of bromine (26.85 g, 0.168 mmol) in carbon tetrachloride (30 mL) and stir at room temperature for 2 days. Quench with a 1M solution of sodium thiosulfate and separate the organic phase. Extract the aqueous phase with carbon tetrachloride, combine the organic phases and dry (MgSO4). Evaporate the solvent in vacuo and purify by distillation to give 3-bromobenzo[b]thiophene as a pale yellow liquid (17.33 g, 48%); bp 64°-72° C. @ 0.02 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05476861 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-8ea860528bc2449592281ceddc95dc08 |
| Source note | uspto-grants-1995_12 |