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Cyclopentanol → (4-Bromobutoxy)cyclopentane

HRID 855566
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HRID 855566 반응식
[H-].[Na+].[CH:3]1([OH:8])[CH2:7][CH2:6][CH2:5][CH2:4]1.[Br:9][CH2:10][CH2:11][CH2:12][CH2:13]Br>C1(C)C=CC=CC=1>[Br:9][CH2:10][CH2:11][CH2:12][CH2:13][O:8][CH:3]1[CH2:7][CH2:6][CH2:5][CH2:4]1
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참가 물질

5

반응물 3

HCID 7298CyclopentanolHCID 80561,4-DibromobutaneHCID 24758Sodium hydride

생성물 1

HCID 21935507(4-Bromobutoxy)cyclopentane

시약·촉매·용매 1

HCID 1140Toluene용매2회

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온도
0 °C

실험 절차

NaH (560 mg, 13.93 mmol, 60% disp. in mineral oil) was washed with hexanes (3×20 mL) in a pressure tube and toluene (6 mL,) was added. The solution was cooled to 0° C. and cyclopentanol (1 g, 11.61 mmol) in toluene (6 mL) was added over 20 min. After stirring at 0° C. for 30 min., 1,4-dibromobutane (1.39 mL, 11.61 mmol) and KI (250 mg) were added. The solution was heated to 100° C. for 14 hours. Upon cooling, the reaction was quenched with NaCl (sat. aq.) and the product extracted with EtOAc. The organic layer was dried over MgSO4, filtered, and concentrated. Purification of the residue via flash column chromatography afforded (4-bromobutoxy)cyclopentane.

후처리

  1. temperatureThe solution was heated to 100° C. for 14 hours
  2. temperatureUpon cooling
  3. customthe reaction was quenched with NaCl (sat. aq.)
  4. extractionthe product extracted with EtOAc
  5. dry with materialThe organic layer was dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customPurification of the residue via flash column chromatography

출처 및 근거

ORD 기록
ord-b21b6695690b4fe69259a0d84059932a
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07262198B2

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