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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thionyl Chloride → [(2-Chloroethyl)selanyl]benzene

HRID 977422
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반응식

HRID 977422 반응식
[C:1]1([Se:7][CH2:8][CH2:9]O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:13])=O>C(Cl)Cl>[Cl:13][CH2:9][CH2:8][Se:7][C:1]1[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 11030856Ethanol, 2-(phenylseleno)-2회

생성물 1

HCID 14699146[(2-Chloroethyl)selanyl]benzene

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

One gram of the resulting 2-hydroxyethyl phenyl selenide was dissolved in 15 ml of CH2Cl2. One ml of thionyl chloride was dissolved in 5 ml of CH2Cl2 and was added to the solution of the 2-hydroxyethyl phenyl selenide. The reaction mixture was refluxed for 1 h. The solvent was evaporated off and the remaining product transferred to a separatory funnel using CHCl3. Twenty ml of water was added to the separatory funnel and was made weakly basic with 5% aqueous NaHCO3. The CHCl3 layer was removed from the separatory funnel, dried with sodium sulfate and removed from the product by rotary evaporation and then in vacuo.

후처리

  1. temperatureThe reaction mixture was refluxed for 1 h
  2. customThe solvent was evaporated off
  3. customthe remaining product transferred to a separatory funnel
  4. additionTwenty ml of water was added to the separatory funnel
  5. customThe CHCl3 layer was removed from the separatory funnel
  6. dry with materialdried with sodium sulfate
  7. customremoved from the product by rotary evaporation

출처 및 근거

ORD 기록
ord-d7b4543fe6064b96a7353b5e431836e3
출처 데이터셋
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05614562

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