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Diethyl Ether → HCID 22908389, 화합물

HRID 1079013
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반응식

HRID 1079013 반응식
[Si]([O:8][CH:9]1[CH2:13][C:12](=[CH2:14])[C:11]([CH:15]([CH3:18])[CH:16]=[CH2:17])=[CH:10]1)(C(C)(C)C)(C)C.CCOCC>O1CCCC1>[CH3:18][CH:15]([C:11]1[C:12](=[CH2:14])[CH2:13][CH:9]([OH:8])[CH:10]=1)[CH:16]=[CH2:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3283Diethyl EtherHCID 22908410HCID 22908410, 화합물

생성물 1

HCID 22908389HCID 22908389, 화합물수율 91%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

2.02 Grams of (RS)-3-(1-methyl-2-propenyl)-4-methylidenecyclopent-2-en-1-yl t-butyldimethylsilyl ether was dissolved in 20 ml of tetrahydrofuran. Under ice-water cooling, 7.7 ml of a tetrahydrofuran solution of 1M n-tetrabutylammonium fluoride was added to the ether solution, and then stirred at an ambient temperature for six hours. The reaction solution was poured into ice-water and extracted with ether. The ether layer was washed with a saturated sodium chloride solution, and dried with anhydrous magnesium sulfate. After removal of the solvent under reduced pressure, the oily substance obtained was subjected to silica gel column chromatography to yield 1.05 g of (RS)-3-(1-methyl-2-propenyl)-4-methylidenecyclopent-2-en-1-ol.

후처리

  1. extractionextracted with ether
  2. washThe ether layer was washed with a saturated sodium chloride solution
  3. dry with materialdried with anhydrous magnesium sulfate
  4. customAfter removal of the solvent under reduced pressure
  5. customthe oily substance obtained

출처 및 근거

ORD 기록
ord-3927df5786aa475498c2c7364156a5b3
출처 데이터셋
uspto-grants-1996_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05550258

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