Potassium Hydroxide → 4-tert-Butylphenylacetylene

HRID 36354

반응식

HRID 36354 반응식
C[Si]([C:5]#[C:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]([CH3:16])([CH3:15])[CH3:14])=[CH:9][CH:8]=1)(C)C.[OH-].[K+]>C(O)(C)C>[C:13]([C:10]1[CH:9]=[CH:8][C:7]([C:6]#[CH:5])=[CH:12][CH:11]=1)([CH3:16])([CH3:15])[CH3:14]

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 14989664((4-(tert-Butyl)phenyl)ethynyl)trimethylsilane2회

생성물 1

HCID 27573024-tert-Butylphenylacetylene

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

To a stirred solution of 1.44 g (6.23 mmol) of trimethylsilyl (4-tert-butyl)phenylethyne (Compound 21) in 5 ml of isopropanol was added 10 ml of 1N aqueous KOH and the mixture then stirred at room temperature for 6.5 hours. The isopropanol was removed under vacuum and the residue extracted with ether. The ether extract was washed with dilute HCl until the washings were acidic. The ether solution was then successively washed with water, saturated NaCl and NaHCO3 solutions and then dried (MgSO4). Solvent was then removed in-vacuo to give the title compound as a colorless oil. PMR (CDCl3): & 1.34 (9H, s), 3.05 (1H, s), 7.37 (2H, d, J~8.2 Hz), 7.46 (2H, d, J~8.2 Hz).

후처리

  1. customThe isopropanol was removed under vacuum
  2. extractionthe residue extracted with ether
  3. extractionThe ether extract
  4. washwas washed with dilute HCl until the washings
  5. washThe ether solution was then successively washed with water, saturated NaCl and NaHCO3 solutions
  6. dry with materialdried (MgSO4)
  7. customSolvent was then removed in-vacuo

출처 및 근거

ORD 기록
ord-56bcecd8013644ed8db0cea27283d819
출처 데이터셋
uspto-grants-1995_05
특허 번호
US05414007

연결된 노트

불러오는 중…