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Trichloromethylsilane → Tetramethylcyclopentadienyl methyl silicon dichloride

HRID 841111
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HRID 841111 반응식
[CH3:1][C:2]1[CH:3]([Li])[C:4]([CH3:9])=[C:5]([CH3:8])[C:6]=1[CH3:7].[CH3:11][Si:12](Cl)([Cl:14])[Cl:13]>C1COCC1>[CH3:1][C:2]1[CH:3]([Si:12]([Cl:14])([Cl:13])[CH3:11])[C:4]([CH3:9])=[C:5]([CH3:8])[C:6]=1[CH3:7]
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참가 물질

4

반응물 2

HCID 6399TrichloromethylsilaneHCID 178506838Lithium tetramethylcyclopentadienide

생성물 1

HCID 11322281Tetramethylcyclopentadienyl methyl silicon dichloride수율 82%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
-78 °C

실험 절차

(2,3,4,5-Tetramethylcyclopentadienyl)lithium (1.33 g, 10.37 mmol) was dissolved in 80 mL THF and cooled to −78° C., and MeSiCl3 (1.70 g, 11.4 mmol) was added via a syringe. After addition, the cooling bath was removed and the reaction mixture was stirred at room temperature for 16 h. Volatiles were removed under vacuum at room temperature, and the residue was extracted twice with hexanes (2×20 mL). The hexane fractions were combined and the solvent was removed under vacuum to give a pale yellow oil (tetramethylcyclopentadienyl methyl silicon dichloride); 2.0 g, 82% yield. 1H-NMR (C6D6): δ (ppm): 2.95 (broad s, 1 H; Me4CpH), 1.92 (s, 6H;), 1.63 (s, 6H; Me4Cp), 0.19 (s, 3 H; MeSi).

후처리

  1. additionAfter addition
  2. customthe cooling bath was removed
  3. customVolatiles were removed under vacuum at room temperature
  4. extractionthe residue was extracted twice with hexanes (2×20 mL)
  5. customthe solvent was removed under vacuum

출처 및 근거

ORD 기록
ord-cf7da4c08a8b49a2ab659941f2df4ca2
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06369253B1

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