HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063939Generated: October 29, 2026
Carbon tetrabromide → HCID 53747118, compound
https://huagongshe.com/reaction/1063939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 53964382 | HCID 53964382 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 53747118 | HCID 53747118 | 84% |
Reaction Steps
To a solution of 4-chloro-N-[5-chloro-2-(acetoxymethyl)phenyl]-N-[(R)-1-methyl-4-hydroxybutyl]benzenesulfonamide (500 mg, 1.09 mmol) in acetonitrile (2 mL) was added triphenylphosphine (571 mg, 2.18 mmol) and carbon tetrabromide (720 mg, 2.18 mmol) at 0° C. The resulting mixture was allowed to stir at 22° C. for 12 h followed by the addition of 25 mL of sat. ammonium chloride. The product was extracted with ether (2×25 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure. Silica gel chromatography (1:4 ethyl acetate:hexanes) of the concentrate afforded 479 mg of 4-chloro-N-[5-chloro-2-(acetoxymethyl)phenyl]-N-[(R)-1-methyl-4-bromobutyl]benzenesulfonamide as a colorless oil in 84% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06967196B1 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-793c86805d5548eea18db9380d625f99 |
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| Source note | uspto-grants-2005_11 |
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