HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759670Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 131724696, compound
https://huagongshe.com/reaction/1759670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 6103705 | HCID 6103705 | — |
| Solvent | Acetonitrile methylene chloride | HCID 21877088 | — |
| Product | HCID 131724696 | HCID 131724696 | — |
Reaction Steps
1.0 mmole of dimethyl sulfoxide is dissolved in dichloromethane/acetonitrile solution, wherein the mole ratio for dichloromethane to acetonitrile is 1:1. Thereafter, the dichloromethane/acetonitrile solution that comprises the dimethyl sulfoxide is placed in a reactor. 1.0 mmole of (tri(2,2,6,6-tetramethyl-3,5-heptanedionate) Tb(III), Tb(TMHD)3 is also placed in the reactor, and a nitrogen gas is introduced into the reactor. The solution is subjected to thermal reflux for 2 hours and is then cooled to room temperature. Thereafter, the solvent is extracted with a rotary vacuum evaporator until the final volume of the solution is half of the original volume and when sediment is formed. After filtering the sediment, the filtered sediment is re-crystallized with methylcyclohexane to obtain the Tb(TMHD)3—DMSO) complex compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06838019B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-a5707de104ab4701846526256d5d08bf |
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| Source note | uspto-grants-2005_01 |
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