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Carbon Tetrachloride → (Z,Z)-1-chloro-2,5-undecadiene

HRID 236035
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HRID 236035 반응식
[CH:1](/O)=[CH:2]/[CH:3]=[CH:4]\[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CCCCCC.C(Cl)(Cl)(Cl)[Cl:39]>>[Cl:39][CH2:1]/[CH:2]=[CH:3]\[CH2:4]/[CH:5]=[CH:6]\[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]
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참가 물질

5

반응물 4

HCID 5943Carbon TetrachlorideHCID 8058HexaneHCID 11776TriphenylphosphineHCID 86738537(Z,Z)-undecadien-1-ol

생성물 1

HCID 13044960(Z,Z)-1-chloro-2,5-undecadiene수율 92%

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온도
23 °C

실험 절차

A mixture of (Z,Z)-undecadien-1-ol (3.42 g, 20.4 mmol) and triphenylphosphine (7.5 g, 28.6 mmol) in dry CCl4 (25 ml) was refluxed with stirring for 9 h. The reaction mixture was allowed to cool to 23° C., hexane (60 ml) was added, and stirring was continued for an additional 10 minutes. The precipitate of triphenylphosphine oxide was filtered and washed with hexane. The solvent was removed from the combined filtrate at 40° C./~30 mm Hg. Evaporative distillation of the resulting residue at 125°-130° C./0.3 mm Hg gave 3.5 g (92%) of (Z,Z)-1-chloro-2,5-undecadiene as a colorless liquid.

후처리

  1. temperaturewas refluxed
  2. stirringstirring
  3. waitwas continued for an additional 10 minutes
  4. filtrationThe precipitate of triphenylphosphine oxide was filtered
  5. washwashed with hexane
  6. customThe solvent was removed from the combined filtrate at 40° C./~30 mm Hg
  7. distillationEvaporative distillation of the resulting residue at 125°-130° C./0.3 mm Hg

출처 및 근거

ORD 기록
ord-5469bd2725b8466b9d62dfbaa632e0ff
출처 데이터셋
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04642364

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