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Thionyl Chloride → 2-(7-Methoxynaphthalen-1-yl)acetyl chloride

HRID 483391
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인쇄 미리보기

반응식

HRID 483391 반응식
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][CH:9]=[C:10]2[CH2:13][C:14]([OH:16])=O)=[CH:5][CH:4]=1.S(Cl)([Cl:19])=O>C(Cl)(Cl)Cl>[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][CH:9]=[C:10]2[CH2:13][C:14]([Cl:19])=[O:16])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 135701052-(7-Methoxynaphthalen-1-yl)acetic acid

생성물 1

HCID 193857662-(7-Methoxynaphthalen-1-yl)acetyl chloride

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

The (7-methoxynaphth-1-yl)acetic acid obtained above is dissolved by heating in 300 ml of chloroform. The mixture is heated under reflux, and then thionyl chloride is added dropwise. The mixture is refluxed for two hours and evaporated to dryness. An oil is obtained which crystallizes on cooling. The residue obtained is used as such in the following stage.

후처리

  1. dissolutionabove is dissolved
  2. temperatureThe mixture is heated
  3. temperatureunder reflux
  4. temperatureThe mixture is refluxed for two hours
  5. customevaporated to dryness
  6. customAn oil is obtained which
  7. customcrystallizes
  8. temperatureon cooling
  9. customThe residue obtained

출처 및 근거

ORD 기록
ord-a5644afb33d14df0ac29383062107646
출처 데이터셋
uspto-grants-1993_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05225442

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