HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477895Generated: October 30, 2026
1,2-Diiodoethane → HCID 14405318, compound
https://huagongshe.com/reaction/477895
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Diiodoethane | HCID 12224 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 15179913 | HCID 15179913 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 14405318 | HCID 14405318 | — |
Reaction Steps
A solution of 2.3 grams (0.012 mole of 2-(4-chloro(phenyl)thiazole in 20 ml of diethyl ether was cooled to -78° C. To this solution was added 4.72 ml of a 2.5 M solution of n-butyllithium in hexanes. This mixture was stirred for 30 minutes. A solution of 3.3 grams (0.012 mole) of 1,2-diiodoethane in 15 ml of diethyl ether was added, and the resultant mixture was allowed to warm to room temperature and stir for approximately 18 hours. Approximately 50 ml of an aqueous, saturated ammonium chloride solution was added, and the resultant mixture was poured into a separatory funnel. The organic phase was washed with water followed by an aqueous, saturated sodium chloride solution. The washed organic phase was dried over anhydrous sodium sulfate and was filtered. The filtrate was evaporated under reduced pressure leaving a residue. This residue was purified by column chromatography on silica gel, eluting with methylene chloride:n-hexane (3:1), to yield 2.6 grams of 2-(4-chlorophenyl)- 5-iodothiazole as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04889867 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-15e52181ae834ee2853fdc5543acb2cb |
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| Source note | uspto-grants-1989_12 |
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