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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Iodide → (R)-5-acetoxy-1-iodohexane

HRID 1421239
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HRID 1421239 반응식
[C:1]([O:4][C@H:5]([CH3:11])[CH2:6][CH2:7][CH2:8][CH2:9]Cl)(=[O:3])[CH3:2].[I-:12].[Na+]>>[C:1]([O:4][C@H:5]([CH3:11])[CH2:6][CH2:7][CH2:8][CH2:9][I:12])(=[O:3])[CH3:2]
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참가 물질

3

반응물 2

HCID 5238Sodium IodideHCID 110194345-(R)-Acetoxy-1-chlorohexane

생성물 1

HCID 54009360(R)-5-acetoxy-1-iodohexane

실험 절차

First, (R)-5-acetoxy-1-iodohexane was prepared in the following manner. A solution of (R)-5-acetoxy-1-chlorohexane (4.80 g:26.89 mmol) was added to sodium iodide (5.39 g:36 mmol) in a round bottomed flask fitted with magnetic stirrer bar and a reflux condenser and refluxed for 12 hrs with stirring. Acetone was removed under reduced pressure, The crude product was partitioned between ethyl acetate (50 ml) and water layer (60 ml). The organic layer was washed with 10% sodium thiosulphate solution followed by water (20 l), dried over anhydrous Mg SO4 and concentrated under reduced pressure. Yield=7 g (96%)

후처리

  1. customfitted with magnetic stirrer bar and a reflux condenser
  2. temperaturerefluxed for 12 hrs
  3. customAcetone was removed under reduced pressure
  4. customThe crude product was partitioned between ethyl acetate (50 ml) and water layer (60 ml)
  5. washThe organic layer was washed with 10% sodium thiosulphate solution
  6. dry with materialdried over anhydrous Mg SO4
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-8023ee2153144af6bd5ffc00179b81c6
출처 데이터셋
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06075029

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