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Sodium Iodide → 4-(Iodomethyl)benzyltri-n-butylammonium iodide

HRID 2399651
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반응식

HRID 2399651 반응식
Cl[CH:2](Cl)[C:3]1[CH:8]=[CH:7][C:6]([CH3:9])=[CH:5][CH:4]=1.[I-:11].[Na+].[CH2:13]([N:17]([CH2:22][CH2:23][CH2:24][CH3:25])[CH2:18][CH2:19][CH2:20][CH3:21])[CH2:14][CH2:15][CH3:16]>CC(C)=O>[I-:11].[I:11][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][N+:17]([CH2:13][CH2:14][CH2:15][CH3:16])([CH2:18][CH2:19][CH2:20][CH3:21])[CH2:22][CH2:23][CH2:24][CH3:25])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 5238Sodium IodideHCID 7622TributylamineHCID 5200171-(Dichloromethyl)-4-methylbenzene

생성물 1

HCID 190321734-(Iodomethyl)benzyltri-n-butylammonium iodide

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a mixture of α,α-dichloro-p-xylene (50 g, 28.6 mmol) and sodium iodide (8.6 g, 57 mmol) in acetone (100 mL) was added tri-n-butylamine (3.7 g, 20.0 mmol). The reaction mixture was stirred at room temperature under argon for several days after which time TLC examination showed completion of the reaction. The reaction mixture was filtered and the solvent was removed under reduced pressure to give an oily residue. The residue was washed with pentane several times and dried to give a yellow solid. The product was used without further purification.

후처리

  1. customcompletion of the reaction
  2. filtrationThe reaction mixture was filtered
  3. customthe solvent was removed under reduced pressure
  4. customto give an oily residue
  5. washThe residue was washed with pentane several times
  6. customdried
  7. customto give a yellow solid
  8. customThe product was used without further purification

출처 및 근거

ORD 기록
ord-35b0271b01604584bf1fc816cb15c481
출처 데이터셋
uspto-grants-1995_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05451347

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