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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Iodide → Isopropoxycarbonyloxyethyl iodide

HRID 248211
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HRID 248211 반응식
[CH:1]([O:4][C:5]([O:7][CH2:8][CH2:9]Cl)=[O:6])([CH3:3])[CH3:2].[I-:11].[Na+]>[Cl-].[Zn+2].[Cl-].C(Cl)(Cl)(Cl)Cl>[CH:1]([O:4][C:5]([O:7][CH2:8][CH2:9][I:11])=[O:6])([CH3:3])[CH3:2]
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참가 물질

5

반응물 2

HCID 5238Sodium IodideHCID 197651192-Chloroethyl propan-2-yl carbonate

생성물 1

HCID 19765127Isopropoxycarbonyloxyethyl iodide수율 57.2%

시약·촉매·용매 2

HCID 3007855Zincchloride촉매HCID 5943Carbon Tetrachloride용매

실험 절차

A mixture of isopropoxycarbonyloxyethyl chloride (=2-chloroethyl isopropylcarbonate) (1.67 g), carbon tetrachloride (10 ml), sodium iodide (2.10 g) and anhydrous zinc chloride (0.08 g) is stirred at room temperature for 2 hours, and thereafter, ice water is added to the mixture. The organic layer is separated, and the aqueous layer is extracted twice.with carbon tetrachloride. The combined organic layers are washed, dried and evaporated under reduced pressure to give isopropoxycarbonyloxyethyl iodide (=2-iodoethyl isopropylcarbonate) (1.48 g) as an oil.

후처리

  1. customThe organic layer is separated
  2. extractionthe aqueous layer is extracted twice.with carbon tetrachloride
  3. washThe combined organic layers are washed
  4. customdried
  5. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-89e5832df91a4a02a5a9d6bf1742368b
출처 데이터셋
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05208348

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