HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288616Generated: November 2, 2026
Triphenylphosphine → HCID 18699969, compound
https://huagongshe.com/reaction/2288616
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1,2-Dibromo-1,1,2,2-tetrachloroethane | HCID 69426 | — |
| Reactant | Benzyl isocyanate | HCID 76639 | — |
| Reactant | HCID 55213626 | HCID 55213626 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 18699969 | HCID 18699969 | 33.1% |
Reaction Steps
0.13 ml (1.05 mmol) of benzyl isocyanate was added to 25 ml of acetonitrile solution containing 253 mg (1.0 mmol) of 2-(hexahydro-1H-azepin-1-yl)methylthiophene-5-carboxylic acid hydrazide, and the mixture was stirred at room temperature for 40 hours, 718 mg (2.2 mmol) of 1,2-dibromo-1,1,2,2-tetrachloroethane, 1.22 ml of triethylamine and 1.16 g of triphenylphosphine were added, and then the mixture was stirred at room temperature for 9 hours. The reaction solution was concentrated, chloroform was added to the resulting residue, followed by washing with water and drying over anhydrous magnesium sulfate. The solvent was evaporated and the resulting residue was purified by a silica gel column chromatography to give 122 mg of the title compound in its free form. By subjecting 117 mg of this compound to salt formation using 27 mg of oxalic acid, 122 mg of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090804 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-b371c08c92584626815121af23bc7e69 |
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| Source note | uspto-grants-2000_07 |
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