HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910383Generated: October 29, 2026
HCID 66783884, compound → HCID 86611476, compound
https://huagongshe.com/reaction/910383
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66783884 | HCID 66783884 | — |
| Reactant | HCID 178477747 | HCID 178477747 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86611476 | HCID 86611476 | — |
Reaction Steps
In 10 ml of a solution of 1-trifluoromethylethenyl zinc bromide prepared according to the method described in documents in 1M tetrahydrofuran, 1.0 g of 3-bromodifluoromethoxy-1-iodobenzene and 0.05 g of dichlorobis(triphenylphosphine) palladium (II) were added, and stirred under reflux with heat for 2 hours. After the completion of the reaction, the reaction mixture was poured in 20 ml of diluted hydrochloric acid, extracted with ethyl acetate (50 ml×1). The organic phase was dehydrated with saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue was dissolved in hexane, and high polar impurities were excluded by treating with silica gel to obtain 0.77 g of crude aimed product as colorless oily substance. The resulting product was used as such without purification for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022089B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-db076cc18b97483c8903aed7638a9b62 |
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| Source note | uspto-grants-2011_09 |
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