HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293839Generated: October 29, 2026
Carbon tetrabromide → HCID 14621980, compound
https://huagongshe.com/reaction/2293839
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 14621979 | HCID 14621979 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Chlorine | HCID 24526 | — |
| Product | HCID 14621980 | HCID 14621980 | 102.2% |
Reaction Steps
A solution of carbon tetrabromide (2,204 gm, 6.65 mmol) in CH2 Cl2 (8 ml) was added over a 12 minute period to a cold (-12° C.) solution of 4-(4-fluorophenyl)-2-(1-methylethyl)-6-phenyl-3-pyridinecarboxaldehyde (1.415 gm, 4.43 mmol) (the preparation of which is described in Example 1) and triphenylphosphine (3,488 gm, 13.3 mmol) in CH2Cl2 (25 ml). After the addition was complete, the cooling bath was removed and the mixture was stirred for 20 minutes. The solution was quenched with saturated NaHCO3 and extracted 3× with CH2Cl2. The combined organic layers were washed with saturated NaHCO3, dried (Na2SO4), filtered and stripped to give a yellow oil. The oil was chromatographed (flash, Merck SiO2, 40% CH2Cl2 in hexane) to give 3-(2,2-dibromoethenyl)-4-(4-fluorophenyl)-2-(1-methylethyl)-6-phenylpyridine as a colorless foam (2.152 gm, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05686433 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-e799fc325e844d5b94dd6d0a4b5f84c9 |
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| Source note | uspto-grants-1997_11 |
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