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Sodium bis(trimethylsilyl)amide → (Z)-3-Ethyl-3-methyl-1-iodo-1-pentene

HRID 636898
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HRID 636898 반응식
[I-].[I:2][CH2:3][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C[Si]([N-][Si](C)(C)C)(C)C.[Na+].[CH2:33]([C:35]([CH3:40])([CH2:38][CH3:39])[CH:36]=O)[CH3:34]>O1CCCC1>[CH2:33]([C:35]([CH3:40])([CH2:38][CH3:39])/[CH:36]=[CH:3]\[I:2])[CH3:34]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 2724254Sodium bis(trimethylsilyl)amideHCID 10973449(Iodomethyl)triphenylphosphonium iodideHCID 15174357HCID 15174357, 화합물

생성물 1

HCID 86756483(Z)-3-Ethyl-3-methyl-1-iodo-1-pentene수율 62%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
-78 °C

실험 절차

A suspension of (iodomethyl)triphenylphosphonium iodide (0.530 g, 1 mmol) in tetrahydrofuran (3 mL) was treated dropwise at room temperature with sodium bis(trimethylsilyl)amide (1 mL, 1M solution in THF, 1 mmol) for 2-3 minutes. The solution was then cooled to −78° C. and a solution of 2-ethyl-2-methyl-butanal (0.100 g, 0.88 mmol) in tetrahydrofuran was added dropwise. The cooling bath was removed and stirring continued at room temperature for 1 hour. The reaction mixture was diluted with hexane, filtered and evaporated. The crude compound was purified by silica gel chromatography (hexane) and afforded the title compound (0.130 g, 62%).

후처리

  1. customThe cooling bath was removed
  2. additionThe reaction mixture was diluted with hexane
  3. filtrationfiltered
  4. customevaporated
  5. customThe crude compound was purified by silica gel chromatography (hexane)

출처 및 근거

ORD 기록
ord-d1d9e937a7434cb29c82c54ec7cda618
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06194601B1

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