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

HRID 67188
ノート
印刷プレビュー

反応式

HRID 67188 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

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

生成物 1

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

反応条件

温度
23 °C

実験手順

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 mmHg. Evaporation distillation of the resulting residue at 125°-130° C./0.3 mmHg gave 3.5 g (92%) of (Z,Z)-1-chloro-2,5-undecadiene as a colorless liquid.

後処理

  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 mmHg
  7. customEvaporation distillation of the resulting residue at 125°-130° C./0.3 mmHg

出典と根拠

ORDレコード
ord-5166ab183bde48ee90f6149d8e21c707
出典データセット
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04345084

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート