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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3,4-dihydro-2H-pyran → 2H-Pyran, tetrahydro-2-[(3-methyl-3-butenyl)oxy]-

HRID 1195634
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HRID 1195634 반응식
[CH:1]([OH:6])=[CH:2][C:3](=[CH2:5])[CH3:4].[O:7]1[CH:12]=[CH:11][CH2:10][CH2:9][CH2:8]1.C(N(CC)CC)C>C(Cl)Cl.CS(O)(=O)=O>[CH3:5][C:3](=[CH2:4])[CH2:2][CH2:1][O:6][CH:8]1[CH2:9][CH2:10][CH2:11][CH2:12][O:7]1
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참가 물질

6

반응물 3

HCID 80803,4-dihydro-2H-pyranHCID 8471TriethylamineHCID 71353452HCID 71353452, 화합물

생성물 1

HCID 122906552H-Pyran, tetrahydro-2-[(3-methyl-3-butenyl)oxy]-수율 100.5%

시약·촉매·용매 2

HCID 6395Methanesulfonic Acid촉매HCID 6344Dichloromethane용매

실험 절차

To isoprenyl alcohol (80.0 g, 929 mmol) in CH2Cl2 (500 ml) at 0° C. was added one drop of methanesulfonic acid. To this solution was added 2,3-dihydropyran (100 ml, 1.10 mol) dropwise over 3 h. After the addition was complete triethylamine (5 ml) was added and the resulting mixture was filtered through a thin pad of SiO2 and concentrated to afford 159 g (100%) of 2-(3-methyl-3-butenyloxy)tetrahydropyran as a colorless liquid.

후처리

  1. additionAfter the addition
  2. additionwas added
  3. filtrationthe resulting mixture was filtered through a thin pad of SiO2
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-d0beb8aeaabb4b1095ae2b8dbb94e40e
출처 데이터셋
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05112595

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