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Acetylene → 1-Chloro-trans-1-octen-3-one

HRID 436092
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HRID 436092 반응식
[Cl-:1].[Al+3].[Cl-].[Cl-].[CH:5]#[CH:6].[C:7](Cl)(=[O:13])[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]>C(Cl)(Cl)(Cl)Cl>[Cl:1]/[CH:5]=[CH:6]/[C:7](=[O:13])[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6326AcetyleneHCID 67340Hexanoyl chlorideHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 110410031-Chloro-trans-1-octen-3-one

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

To a slurry of 233.5 g. (1.75 moles) of aluminum chloride in 390 ml. of carbon tetrachloride, saturated with acetylene and cooled in an ice bath, is added over 20 minutes 201.9 g. (1.50 moles) of hexanoyl chloride. After the addition is complete, acetylene is bubbled into the mixture as rapidly as it is absorbed and for 1 hour after absorption becomes slow. The mixture is poured onto 1700 g. of ice and 720 ml. of saturated brine. The organic phase is separated and the aqueous phase is washed with ether. The combined organic phase and washings are washed with saturated brine, dried (Na2SO4) and evaporated. The residual oil is combined with 10 g. of hydroquinone and distilled to yield a colorless oil, b.p. 51°-52° C. (0.10 torr).

후처리

  1. additionis added over 20 minutes 201.9 g
  2. additionAfter the addition
  3. customacetylene is bubbled into the mixture as rapidly as it
  4. customis absorbed and for 1 hour
  5. customafter absorption
  6. additionThe mixture is poured onto 1700 g
  7. customThe organic phase is separated
  8. washthe aqueous phase is washed with ether
  9. washThe combined organic phase and washings are washed with saturated brine
  10. dry with materialdried (Na2SO4)
  11. customevaporated
  12. distillationof hydroquinone and distilled
  13. customto yield a colorless oil, b.p. 51°-52° C. (0.10 torr)

출처 및 근거

ORD 기록
ord-85cd40821ba3482dad2d2fec0f158f7d
출처 데이터셋
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04007210

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