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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethylene → 8-Bromo-1,2,3,4-tetrahydronaphthalen-2-one

HRID 728074
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HRID 728074 반응식
[Cl-].[Al+3].[Cl-].[Cl-].[Br:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[CH2:12][C:13](Cl)=[O:14].[CH2:16]=[CH2:17]>C(Cl)Cl>[Br:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:7]=1[CH2:12][C:13](=[O:14])[CH2:17][CH2:16]2
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참가 물질

5

반응물 3

HCID 6325EthyleneHCID 41383862-Bromophenylacetyl chlorideHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 41361878-Bromo-1,2,3,4-tetrahydronaphthalen-2-one

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

83.5 g of aluminum chloride (0.63 mmol) were introduced into 1.8 liters of methylene chloride at 0°-+5° C. 105 g (0.49 mole) of 2-bromophenyl-acetyl chloride (dissolved in 200 ml of methylene chloride) were added dropwise at 0°-+5° C. over 30 minutes. After stirring for 30 minutes at 0°-+5° C., 50 g of ethylene were passed in at such a rate that the reaction temperature did not exceed +10° C. The mixture was stirred for a further 2 hours at 20°-+25° C. The aluminum complex was decomposed by careful addition of 500 ml of ice water, the phases were separated, and the aqueous phase was extracted with 250 ml of methylene chloride. The title compound was obtained from the dried methylene chloride phase in a yield of 109 g as a yellow oil (content according to GC 97%) and employed without further purification.

후처리

  1. customdid not exceed +10° C
  2. stirringThe mixture was stirred for a further 2 hours at 20°-+25° C
  3. customthe phases were separated
  4. extractionthe aqueous phase was extracted with 250 ml of methylene chloride

출처 및 근거

ORD 기록
ord-466ce25420ef495b813c28d665abd854
출처 데이터셋
uspto-grants-1991_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05047422

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