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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thionyl Chloride → 2-(7-Methoxynaphthalen-1-yl)acetyl chloride

HRID 274758
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인쇄 미리보기

반응식

HRID 274758 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-ylacetic acid obtained above is dissolved, while warm, in 300 cm3 of chloroform. The mixture is heated to reflux, and then thionyl chloride is added dropwise. The mixture is refluxed for two hours and evaporated to dryness, yielding an oil which crystallises by cooling. The resulting residue is used as such in the following step.

후처리

  1. dissolutionis dissolved
  2. temperatureThe mixture is heated
  3. temperatureto reflux
  4. temperatureThe mixture is refluxed for two hours
  5. customevaporated to dryness
  6. customyielding an oil which
  7. customcrystallises
  8. temperatureby cooling

출처 및 근거

ORD 기록
ord-68b8a011210c4d8fbc1f976d53140819
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05389683

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