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Diethyl Ether → 2-(5-Bromopentyl)oxirane

HRID 420841
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HRID 420841 반응식
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH:7]=[CH2:8].ClC1C=CC=C(C(OO)=[O:17])C=1.C(OCC)C.S([O-])([O-])(=O)=S.[Na+].[Na+]>C(Cl)(Cl)Cl>[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH:7]1[CH2:8][O:17]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 3283Diethyl EtherHCID 24477Sodium ThiosulfateHCID 70297m-Chloroperbenzoic acidHCID 5244507-Bromo-1-heptene

생성물 1

HCID 142253782-(5-Bromopentyl)oxirane수율 94.8%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

7-Bromo-1-heptene (5.10 g) was dissolved in chloroform (29 ml), the solution was added with m-chloroperbenzoic acid (6.21 g) under ice cooling, and the mixture was stirred at room temperature for 3 hours. The reaction mixture was added with diethyl ether and saturated aqueous sodium thiosulfate, the layers were separated, and the organic layer was washed with saturated aqueous sodium hydrogencarbonate, then dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under ordinary pressure to obtain the title compound (5.27 g).

후처리

  1. customthe layers were separated
  2. washthe organic layer was washed with saturated aqueous sodium hydrogencarbonate
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated under ordinary pressure

출처 및 근거

ORD 기록
ord-0681951f2ced40f491ea062d87d9dc12
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08097708B2

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