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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440566Generated: November 2, 2026

Iodoethane → 2-Chloro-N-(2-ethoxyethyl)-N-ethyl-6-(trimethylsilyl)benzamide

https://huagongshe.com/reaction/1440566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantN-(2-ethoxyethyl)-2-chloro-6-(trimethylsilyl)benzamideHCID 18630026—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-N-(2-ethoxyethyl)-N-ethyl-6-(trimethylsilyl)benzamideHCID 1863021683%

Reaction Steps

A 1M THF solution of sodium bis(trimethylsilyl)-amide (7.7 mL, 7.7 mmol) was added dropwise over 5 min to a solution of N-(2-ethoxyethyl)-2-chloro-6-(trimethylsilyl)benzamide (2.1 g, 7 mmol) in THF (30 mL). The resulting mixture was stirred for 1 h at RT, then a solution of ethyl iodide (1.31 g, 8.4 mmol) in THF (15 mL) was added with a mild exotherm. The resulting reaction mixture was stirred overnight, then was partitioned between ethyl acetate and dilute aq citric acid. The ethyl acetate phase was washed with sat aq NaHCO3 followed with brine, then was dried (MgSO4) and concentrated to afford 1.9 g of the title compound as an amber oil, an 83% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498630
Source datasetuspto-grants-1996_03
ORD IDord-37f780e7229149659b43659588ba286d
Source noteuspto-grants-1996_03