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Thionyl Chloride → 1-(Chloromethyl)-4-(4-phenylbutoxy)benzene

HRID 1739403
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인쇄 미리보기

반응식

HRID 1739403 반응식
[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][O:11][C:12]2[CH:19]=[CH:18][C:15]([CH2:16]O)=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:22])=O>C(Cl)(Cl)Cl>[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][O:11][C:12]2[CH:19]=[CH:18][C:15]([CH2:16][Cl:22])=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 540346054-(4-Phenylbutoxy)benzyl alcohol

생성물 1

HCID 151155321-(Chloromethyl)-4-(4-phenylbutoxy)benzene수율 102.9%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

2.9 g of 4-(4-phenylbutyloxy)benzyl alcohol were dissolved in 30 ml of chloroform, and 1.6 g of thionyl chloride were further fed dropwise to the resultant solution. The solution was then stirred for 1 hour at room temperature. After completed the reaction, the solution reacted was poured into ice-water and extracted with chloroform. The organic layer resulted was dried with anhydrous magnesium sulfate, and the solvent used was removed by distillation under reduced pressure, thereby affording 3.2 g of 4-(4-phenylbutyloxy)benzyl chloride.

후처리

  1. customthe reaction
  2. customthe solution reacted
  3. extractionextracted with chloroform
  4. customThe organic layer resulted
  5. dry with materialwas dried with anhydrous magnesium sulfate
  6. customthe solvent used was removed by distillation under reduced pressure

출처 및 근거

ORD 기록
ord-e90f10463560454484813b7b1dbc222d
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05965743

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