HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295219Generated: October 31, 2026
Carbon tetrabromide → HCID 15099566, compound
https://huagongshe.com/reaction/2295219
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 21471506 | HCID 21471506 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Chlorine | HCID 24526 | — |
| Product | HCID 15099566 | HCID 15099566 | 99% |
Reaction Steps
A solution of carbon tetrabromide (2.866 gm, 8.64 mmol) in CH2 Cl2 (8 ml) was added over a 10 minute period to a cold (-10° C.) solution of 2-(4-Fluorophenyl)-4-(1-methylethyl)-6-phenyl-3-pyridinecarboxaldehyde (1.840 gm, 5.76 mmol) (the preparation of which is described in Example 3) and triphenylphosphine (4.590 gm, 17.5 mmol) in CH2Cl2 (30 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 2X with CH2Cl2. The combined organic layers were washed with saturated NaHCO3, dried (Na2SO4), filtered and concentrated. The concentrate was chromatographed (flash, Merck, SiO2, 1:1 CH2Cl2 :hexane) to give 3-(2,2-Dibromoethenyl)-2-(4-fluorophenyl)-4-(1-methylethyl)-6-phenylpyridine as a white solid (2.701 gm, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05691322 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-66cdeeffd6c149cd9ce79c617685fb43 |
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| Source note | uspto-grants-1997_11 |
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