HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341756Generated: November 1, 2026
Carbon tetrabromide → HCID 12606990, compound
https://huagongshe.com/reaction/341756
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-[[3-(Trifluoromethyl)phenyl]amino]ethanol | HCID 15636103 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 12606990 | HCID 12606990 | 258.8% |
Reaction Steps
N-(3-trifluoromethylphenyl)ethanolamine (4.17 g) and triphenyl phosphine (5.50 g) were dissolved in dry pyridine (35 ml) and stirred at 0° C. To this solution was added, portionwise, carbon tetrabromide (7.08 g). Stirring was continued for 1 hour and the reaction mixture was left to stand at room temperature overnight. A little more triphenyl phosphine (0.20 g) was added, and when virtually all starting alcohol had been consumed the pyridine was removed under reduced pressure to leave a brown residue (14.10 g). This was chromatographed on silica gel, eluting with ethyl acetate/hexane (1:9) as eluant to give the title compound as a light brown oil, yield 3.35 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05856273 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-c2962ddc9659493684557a5774eb4c15 |
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| Source note | uspto-grants-1999_01 |
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