HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183658Generated: November 4, 2026
Phenyltrimethylammonium bromide dibromide → HCID 22473920, compound
https://huagongshe.com/reaction/2183658
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Reactant | HCID 22473850 | HCID 22473850 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22473920 | HCID 22473920 | 193% |
Reaction Steps
Phenyltrimethylammonium tribromide (1.58 g) was added in portions under nitrogen at 0° C. over 30 minutes to a stirred solution of 1-(4,5-dichlorobenzo[b]thiophen-2-yl)propan-1-one (1.09 g) in tetrahydrofuran (80 ml), then the mixture was stirred at 0° C. for 30 minutes, at ambient temperature for 18 hours and at reflux temperature for 5 hours. Further phenyltrimethylammonium tribromide (0.79 g) was added, the mixture was heated under reflux for 2 hours, then it was cooled to ambient temperature and filtered. The solvent was removed in vacuo to give a brown oil which was purified by flash chromatography over silica using a 3:1 mixture of petroleum ether (b.p. 60-80° C.) and dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to give 2-bromo-1-(4,5-dichlorobenzo[b]thiophen-2-yl)propan-1-one (1.59 g) as an oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900216B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-d2c20d4bce764e53bcccb78baff42640 |
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| Source note | uspto-grants-2005_05 |
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