HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107847Generated: November 1, 2026
HCID 18786094, compound → HCID 18786085, compound
https://huagongshe.com/reaction/1107847
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18786094 | HCID 18786094 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18786085 | HCID 18786085 | 54.5% |
Reaction Steps
A solution of 175 g (0.35 mol) of [(4-fluoro-2-nitrophenyl)methyl]-triphenylphosphonium bromide in 760 mL of EtOH and 380 mL of 48% HBr was brought to reflux and 138 g (2.1 mol) of zinc dust was added in portions over 4 h and refluxed further for 2 h. The mixture was cooled and the EtOH evaporated. The residue was partitioned between CH2Cl2 and H2O. The CH2Cl2 solution was washed with 7M NH4OH. The aqueous phase was decanted and the precipitate dissolved in CH2Cl2 /EtOH. The organic phase was washed with brine, dried (Na2SO4) and concentrated. There was obtained 89 g (54%) of [(2-amino-4-fluorophenyl)methyl]triphenylphosphonium bromide as a solid: 1H NMR (Me2SO-d6) δ 8.0-7.6 (m, 15H); 6.6 (m, 1H); 6.4 (m, 1H); 6.15 (m, 1H); 5.5 (br s, 2H); 4.95 (d, 2H). ##STR17##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06063803 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-d66eb1048e464c5b8e4634355419d595 |
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| Source note | uspto-grants-2000_05 |
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