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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 984694생성일: 2026년 10월 25일

Dodecane → N-(3,5-dimethylphenyl)-N-methylformamide

https://huagongshe.com/reaction/984694

반응식

참여 물질

역할이름HCID투입량
반응물DodecaneHCID 8182—
반응물N-MethylformamideHCID 31254—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물1-Iodo-3,5-dimethylbenzeneHCID 140924—
반응물HCID 178454901HCID 178454901—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물N-(3,5-dimethylphenyl)-N-methylformamideHCID 985556446%

반응 조건

온도110 °C

반응 단계

A Schlenk tube was charged with CuI (9.6 mg, 0.050 mmol, 5.0 mol %), di-tert-butylphosphine oxide (16.5 mg, 0.102 mmol), K3PO4 (430 mg, 2.03 mmol), evacuated, backfilled with Ar. 5-Iodo-m-xylene (145 μL, 1.00 mmol), N-methylformamide (72 μL, 1.23 mmol), and toluene (1.0 mL) were added under Ar. The Schlenk tube was sealed with a Teflon valve and the reaction mixture was stirred at 110° C. for 24 h. The suspension was allowed to reach room temperature. Dodecane (internal GC standard, 230 μL) and ethyl acetate (2 mL) were added. A 0.1 mL sample of the supernatant solution was diluted with ethyl acetate (1 mL) and analyzed by GC to provide a 46% yield of N-(3,5-dimethylphenyl)-N-methylformamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06867298B2
출처 데이터셋uspto-grants-2005_03
ORD IDord-08b3a357a805443f814394c8feec43ff
출처 메모uspto-grants-2005_03