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Sodium Iodide → HCID 20442205, 화합물

HRID 1632748
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HRID 1632748 반응식
[I-:1].[Na+].C1(C)C=CC(S(O[CH2:13][CH:14]([O:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[CH2:15][O:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])(=O)=O)=CC=1>CC(C)=O>[CH2:26]([O:25][CH:14]([CH2:15][O:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH2:13][I:1])[CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5238Sodium IodideHCID 20442238HCID 20442238, 화합물

생성물 1

HCID 20442205HCID 20442205, 화합물수율 79.6%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

Sodium iodide (4.07 g) was added to a stirred solution of 2,3-di-n-octyloxy-1-propyl p-toluenesulfonate (860 mg) in acetone (14 ml) at room temperature and heated under reflux for 11 hours. The resultant mixture was evaporated under reduced pressure, and the residue was dissolved in a mixture of water (20 ml) and diethyl ether (10 ml). The aqueous solution was separated and extracted with diethyl ether, and then the organic layer and the extract were combined. The organic solution was washed with a saturated aqueous solution of sodium chloride twice, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give oil (620 mg) of 2,3-di-n-octyloxy-1-propyl iodide.

후처리

  1. temperatureheated
  2. temperatureunder reflux for 11 hours
  3. customThe resultant mixture was evaporated under reduced pressure
  4. dissolutionthe residue was dissolved in a mixture of water (20 ml) and diethyl ether (10 ml)
  5. customThe aqueous solution was separated
  6. extractionextracted with diethyl ether
  7. washThe organic solution was washed with a saturated aqueous solution of sodium chloride twice
  8. dry with materialdried over anhydrous magnesium sulfate
  9. customThe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-bcf498048abd48a7a3d7b1fc32ed6e5a
출처 데이터셋
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04477447

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