HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745846Generated: October 31, 2026
Iodo benzene diacetate → HCID 131725681, compound
https://huagongshe.com/reaction/1745846
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, 4.5 mg (0.014 mmol) of iodobenzene diacetate was added to a mixture of 5 mg (0.017 mmol) of 4-ferrocenylurazole and 0.25 mL of tetrahydrofuran at room temperature, followed by stirring for an hour. Thus, the tetrahydrofuran solution of 4-ferrocenyl-1,2,4-triazoline-3,5-dione was obtained. A tetrahydrofuran (0.25 mL) solution of 1 mg (0.0025 mmol) of alfacalcidol prepared in accordance with the method described in Japanese Patent Publication (KOKAI) No. 48-62750, Tetrahedron Lett., 1973, 2339 and Tetrahedron, 30, 2701 (1974) was added to the solution obtained. The mixture was stirred at room temperature for an hour. The reaction mixture was concentrated under reduced pressure and the residue obtained was purified by thin layer silica gel chromatography (hexane:ethyl acetate=1:2) to give 1 mg (57%) of the titled alfacalcidol/4-ferrocenyl-1,2,4-triazoline-3,5-dione adduct (ALF-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-bf377aa933104135ab4245b941eb1aa4 |
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| Source note | uspto-grants-2006_03 |
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