HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745848Generated: October 31, 2026
Iodo benzene diacetate → HCID 131725681, compound
https://huagongshe.com/reaction/1745848
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Reactant | HCID 178518852 | HCID 178518852 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131725681 | HCID 131725681 | — |
Reaction Steps
With reference to EXAMPLE 1-2, 11 mg (0.034 mmol) of iodobenzene diacetate was added to a mixture of 10 mg (0.035 mmol) of 4-ferrocenylurazole and 0.5 mL of tetrahydrofuran at room temperature. The mixture was stirred for an hour to give the tetrahydrofuran solution of 4-ferrocenyl-1,2,4-triazoline-3,5-dione. A tetrahydrofuran (0.5 mL) solution of 10 mg (0.026 mmol) of cholecalciferol (VD3, manufactured by Solvay Pharmaceutical, Co.) was added to the solution obtained, followed by stirring at room temperature for an hour. The resulting mixture was concentrated under reduced pressure and the residue obtained was purified by thin layer silica gel chromatography (hexane:ethyl acetate=2:1) to give 11 mg (63%) of the titled cholecalciferol/4-ferrocenyl-1,2,4-triazoline-3,5-dione adduct (VD3-FTAD) as a yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07019146B1 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-8d0774022866453c856b7e0a02fe6bc7 |
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| Source note | uspto-grants-2006_03 |
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