Phenylsilane → N-Methyl-2,3-dihydro-1H-inden-1-amine

HRID 486837노트

반응식

HRID 486837 반응식
C([Li])CCC.C1([SiH3])C=CC=CC=1.[CH3:13][N:14]=[C:15]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH2:17][CH2:16]1>C1C=CC=CC=1.[Al].CCOCC.CO>[CH3:13][NH:14][CH:15]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH2:17][CH2:16]1

참가 물질

8

실험 절차

(R,R)-Ethylene-1,2-bis(η5 -4,5,6,7-tetrahydroindenyl) titanium (R)-1,1'-binaphth-2,2'-diolate (30 mg, 0.050 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 (41 μL, 0.065 mmol, 1.6M in hexane) was added and the mixture was shaken until it turned a dark red brown color. After 5 min. phenylsilane, (93 μL, 0.75 mmol) was added and the reaction mixture turned blue, then brown, in color. After 10 min. indanone N-methyl imine (72.6 mg, 0.50 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 20 mL of water and extracted with 1M HCl (2×20 mL). The aqueous layer was separated, basified with 5 M NaOH (until strongly basic to pH paper), and extracted with ether (2×50 mL). The ether solution was dried over anhydrous sodium sulfate and concentrated to yield 65 mg (0.44 mmol, 88% yield) of N-methyl-1-indanamine as a yellow oil.

후처리

  1. stirringThe tube was shaken
  2. stirringto stir for 2 hours
  3. washThe reaction mixture was then washed with 20 mL of water
  4. extractionextracted with 1M HCl (2×20 mL)
  5. customThe aqueous layer was separated
  6. extractionextracted with ether (2×50 mL)
  7. dry with materialThe ether solution was dried over anhydrous sodium sulfate
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-dd78438467de4d0c8a3eb8a64e0b0b21
출처 데이터셋
uspto-grants-1994_03
특허 번호
US05292893

반응 노트

불러오는 중…