Trimethylsilylacetylene → HCID 53804595, 화합물

HRID 275550

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HRID 275550 반응식
C([Li])CCC.[CH3:6][Si:7]([C:10]#[CH:11])([CH3:9])[CH3:8].[CH2:12]([O:14][P:15](Cl)[O:16][CH2:17][CH3:18])[CH3:13]>O1CCCC1>[CH3:6][Si:7]([C:10]#[C:11][P:15]([O:16][CH2:17][CH3:18])[O:14][CH2:12][CH3:13])([CH3:9])[CH3:8]

참가 물질

5

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온도
-20 °C

실험 절차

n-Butyllithium (26.02 ml, 1.55M in hexane) was added dropwise over thirty minutes to a stirred solution of trimethylsilylacetylene (5.18 ml) in dry tetrahydrofuran (25 ml), whilst maintaining the temperature below -65° C. After twenty minutes, diethylchlorophosphite (4.71 ml) was added dropwise over twenty minutes, then stirring continued for a further ninety minutes at -65° C. The stirred mixture was allowed to warm to -20° C., quenched by dropwise addition of saturated ammonium chloride solution (10 ml), then allowed to reach room temperature, diluted with water (10 ml) and extracted with chloroform (4×25 ml). The extracts were dried over magnesium sulphate and evaporated under reduced pressure to give diethyl trimethylsilylethynylphosphonite as a brown oil (7.34 g, 83% pure by GC).

후처리

  1. temperaturewhilst maintaining the temperature below -65° C
  2. waitAfter twenty minutes
  3. waitcontinued for a further ninety minutes at -65° C
  4. customquenched by dropwise addition of saturated ammonium chloride solution (10 ml)
  5. customto reach room temperature
  6. additiondiluted with water (10 ml)
  7. extractionextracted with chloroform (4×25 ml)
  8. dry with materialThe extracts were dried over magnesium sulphate
  9. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-01b0f93d550c45e19bf61efdb1888782
출처 데이터셋
uspto-grants-1995_02
특허 번호
US05393732

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