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Iodic acid → HCID 21266601, 화합물

HRID 610621
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반응식

HRID 610621 반응식
[C:1]1([CH3:19])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[CH2:11][CH2:10][CH2:9]O1.[I:20](O)(=O)=O>>[C:1]1([CH3:19])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH3:18])=[CH:11][CH2:10][CH2:9][I:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24345Iodic acidHCID 21266612HCID 21266612, 화합물

생성물 1

HCID 21266601HCID 21266601, 화합물

실험 절차

A solution of 2,2-di-(2-tolyl)-tetrahydrofuran 33a (40 g) in 57% aqueous iodic acid (250 mL) was boiled under reflux for 30 min. The cooled solution was extracted wiyh diethyl ether. The combined organic phases were washed with water and a saturated aqueous solution of NaCl, dried (Na2SO4) and evaporated in vacuo. The residue was subjected to CC (n-heptane/ethyl acetate 15:1) to give the title compound 36a as an oil (44 g). 1H NMR (CDCl3) δ2.10 (s,3H), 2.30 (s,3H), 2.65 (q,2H), 3.19 (t,2H), 5.73 (t,1H), 7.05-7.22 (m,8H)

후처리

  1. temperatureunder reflux for 30 min
  2. extractionThe cooled solution was extracted wiyh diethyl ether
  3. washThe combined organic phases were washed with water
  4. dry with materiala saturated aqueous solution of NaCl, dried (Na2SO4)
  5. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-2d7d3e14c463462084be05964f4a0163
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05998613

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