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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421102Generated: November 4, 2026

Ammonium Chloride → HCID 131721843, compound

https://huagongshe.com/reaction/1421102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantN-IodosuccinimideHCID 120273—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-thiophen-2-yl-1H-imidazoleHCID 4291023—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131721843HCID 131721843—

Reaction Conditions

Temperature-78 °C

Reaction Steps

1-[2-(trimethylsilyl)ethoxy]methyl]-2-thiophenyl-imidazole (1.06 g, 3.46 mM) was dissolved in 40 ml of dry THF and the solution cooled to -78° C. under N2. Lithium diisopropylamide (3.46 ml, 5.19 mM, 1.5M solution in cyclohexane from Aldrich) was added via syringe, and the reaction solution stirred for 1 hour at -78° C. N-iodosuccinimide (0.85 g, 3.77 mM) in 10 ml of dry THF was added via syringe, and the reaction stirred for 30 minutes. The reaction mixture was added to 200 ml of saturated ammonium chloride, and extracted with 200 ml of ethyl acetate. The ethyl acetate layer was washed with saturated sodium bisulfite solution (150 ml), separated, dried over Na2SO4, filtered, and evaporated in vacuo to give a crude red brown oil. Purification by silica gel column chromatography using ethyl acetate/hexanes 1:9 gave 1.089 grams of 1-[2-(trimethylsilyl)ethoxy]methyl]-2-thiophenyl-5-iodo-imidazole (orange viscous oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06072057
Source datasetuspto-grants-2000_06
ORD IDord-4b9b5b03c50345a0b4f50540b4eed10e
Source noteuspto-grants-2000_06