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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486836생성일: 2026년 10월 25일

Phenylsilane → N-Methyl-1-phenylethylamine

https://huagongshe.com/reaction/486836

반응식

참여 물질

역할이름HCID투입량
반응물PhenylsilaneHCID 12752—
반응물N-Methyl-1-phenylethan-1-imineHCID 576474—
반응물ButyllithiumHCID 178418339—
용매BenzeneHCID 241—
용매MethanolHCID 887—
용매Diethyl EtherHCID 3283—
용매AluminumHCID 5359268—
생성물N-Methyl-1-phenylethylamineHCID 57740350.6%

반응 단계

(R,R)-Ethylene-1,2-bis(η5 -4,5,6,7-tetrahydroindenyl) titanium (R)-1,1'-binaphth-2,2'-diolate (53 mg, 0.089 mmol) was dissolved in 4 mL of dry benzene in a Schlenk tube under a nitrogen atmosphere. The tube was wrapped in aluminum foil. A solution of n-butyllithium (72 μL, 0.12 mmol, 1.6M in hexane) was added and the mixture was shaken until it turned a dark red brown color. After 5 min. phenylsilane, (164 μL, 1.33 mmol) was added and the reaction mixture turned blue, then brown, in color. After 10 minutes acetophenone N-methyl imine (119 mg, 0.89 mmol) was added. The tube was shaken and left for about 20 hours at room temperature. The resulting solution was diluted with 15 mL of ether and 3 mL of methanol and allowed to stir for 2 hours. The reaction mixture was then washed with 10 mL of water and extracted with 1M HCl (2×10 mL). The aqueous layer was separated, basified with 5M NaOH (until strongly basic to pH paper), and extracted with ether (3×20 mL). The ether solution was dried over anhydrous sodium sulfate and concentrated to yield 60 mg (0.45 mmol, 50% yield) of N-methyl-1-phenylethylamine as a yellow oil. The yield for repeated experiments ranged from 50 to 80%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05292893
출처 데이터셋uspto-grants-1994_03
ORD IDord-ebf2d1309f754cd2990d92d2157ae5e2
출처 메모uspto-grants-1994_03