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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Bromopropane → Phosphonium, tetrapropyl-, bromide

HRID 1760070
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HRID 1760070 반응식
[CH3:1][CH2:2][CH2:3][Br:4].[CH2:5]([P:8]([CH2:12][CH2:13][CH3:14])[CH2:9][CH2:10][CH3:11])[CH2:6][CH3:7]>C(#N)C>[Br-:4].[CH2:3]([P+:8]([CH2:12][CH2:13][CH3:14])([CH2:9][CH2:10][CH3:11])[CH2:5][CH2:6][CH3:7])[CH2:2][CH3:1]
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참가 물질

4

반응물 2

HCID 78401-BromopropaneHCID 75226Tripropylphosphine

생성물 1

HCID 11011483Phosphonium, tetrapropyl-, bromide

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

In a 250 mL round bottom flask, n-propyl bromide (21.1 g, 171.5 mmol) (available from Sigma-Aldrich Canada) was dissolved in anhydrous acetonitrile (100 mL) under Ar-atmosphere, and tripropylphosphine (25 g, 156.0 mmol) (available from Sigma-Aldrich Canada) was added. The reaction mixture was heated at gentle reflux for 35 hrs. After cooling to room temperature, the solvent was removed under reduced pressure. The solid residue was suspended in toluene (50 mL) and the solvent was removed under reduced pressure. This process was repeated once. The solid residue was suspended in hexane (100 mL), filtered, washed with hexane (3×50 mL), and air-dried. The desired tetra (n-propyl)phosphonium bromide was obtained as colourless crystals (42.5 g, 96%).

후처리

  1. additionwas added
  2. temperatureThe reaction mixture was heated
  3. temperatureat gentle reflux for 35 hrs
  4. customthe solvent was removed under reduced pressure
  5. customthe solvent was removed under reduced pressure
  6. filtrationfiltered
  7. washwashed with hexane (3×50 mL)
  8. customair-dried

출처 및 근거

ORD 기록
ord-41e12e5a8c934b78aedb093e178ea2cc
출처 데이터셋
uspto-grants-2005_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06838576B1

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