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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980497Generated: November 1, 2026

Iodoethane → HCID 13424103, compound

https://huagongshe.com/reaction/1980497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHexaneHCID 8058—
Reactant1-{[2-(2,4-Dichlorophenyl)-1,3-thiazolidin-2-yl]methyl}-1H-1,2,4-triazoleHCID 13304224—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13424103HCID 13424103—

Reaction Conditions

Temperature-50 °C

Reaction Steps

2.0 g of 2-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazole-1-yl methyl) thiazolidine used in Working Example 7 was dissolved in anhydrous tetrahydrofuran. After cooling the solution to -50° C., 4.5 ml of a n-hexane solution containing 15% of n-butyl lithium was added and the mixture was stirred for 30 minutes at the same temperature. Then, 2.2 g of ethyl iodide was added and the mixture was reacted for 1 hour at the same temperature. Then, the temperature was gradually raised to room temperature. After distilling off tetrahydrofuran under reduced pressure, the reaction product was purified by silica gel column chromatography using a solvent mixture of chloroform and ethyl acetate as the developer, whereby 1.0 g of 2-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazole-1-yl methyl)-3-ethyl thiazolidine (Compound No. 56 in Table 1) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04510154
Source datasetuspto-grants-1985_04
ORD IDord-71575991f03c4bce8f748e93a7cdb7ee
Source noteuspto-grants-1985_04