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3,4-dihydro-2H-pyran → 11-Bromo-1-tetrahydropyranyloxyundecane

HRID 601785
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반응식

HRID 601785 반응식
C1(C)C=CC(S(O)(=O)=O)=CC=1.N1C=CC=CC=1.[Br:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][OH:30].[O:31]1[CH:36]=[CH:35][CH2:34][CH2:33][CH2:32]1>>[Br:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][O:30][CH:32]1[CH2:33][CH2:34][CH2:35][CH2:36][O:31]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 80803,4-dihydro-2H-pyranHCID 7416311-Bromo-1-undecanolHCID 161440Pyridine 4-methylbenzene-1-sulfonate

생성물 1

HCID 1141638811-Bromo-1-tetrahydropyranyloxyundecane

실험 절차

Pyridine toluene 4-sulphonate (1,0 g, 4,0 mmol) and 11-Bromo-1-undecanol (10,0 g, 400 mmol) were dissolved in dry CH2CH2 (200 ml) at ambient temperature, and 3,4-dihydro-2H-pyrane (5,0 g, 60 mmol) was added. The reaction mixture was stirred overnight. The crude product was purified by flash chromatography on silica gel eluted with CH2Cl2. The yield of 11-Bromo-1(tetrahydro-2-pyranyloxy)undecane was 10,7 g (80%).

후처리

  1. customThe crude product was purified by flash chromatography on silica gel
  • washeluted with CH2Cl2
  • 출처 및 근거

    ORD 기록
    ord-91f440436d314e2a95be3ce5b9c82c03
    출처 데이터셋
    uspto-grants-2011_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07902399B2

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