Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745845Generated: October 30, 2026

Iodo benzene diacetate → HCID 129849852, compound

https://huagongshe.com/reaction/1745845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodo benzene diacetateHCID 12217721—
ReactantHCID 178518853HCID 178518853—
SolventTetrahydrofuranHCID 8028—
ProductHCID 129849852HCID 129849852—

Reaction Steps

With reference to EXAMPLE 1-1, 5 mg (0.016 mmol) of iodobenzene diacetate was added to a mixture of 5 mg (0.017 mmol) of 4-(ferrocenylmethyl)urazole and 0.25 mL of tetrahydrofuran at room temperature. The mixture was stirred for 2 hours to give the tetrahydrofuran solution of 4-(ferrocenylmethyl)-1,2,4-triazoline-3,5-dione. 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 resulting solution, 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=1:2) to give 1 mg (57%) of the titled alfacalcidol/4-(ferrocenylmethyl)-1,2,4-triazoline-3,5-dione adduct (ALF-FMTAD) as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019146B1
Source datasetuspto-grants-2006_03
ORD IDord-bb43aef7b4f04809a48615bc3938042c
Source noteuspto-grants-2006_03