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Pentane → Benzene, (3-methyl-3-buten-1-ynyl)-

HRID 369442
ノート
印刷プレビュー

反応式

HRID 369442 の反応式
[CH3:1][C:2]([CH:4](O)[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[CH2:3].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CCCCC>O1CCCC1.C(Cl)(Cl)(Cl)Cl>[CH3:3][C:2]([C:4]#[C:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[CH2:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 8003PentaneHCID 11776TriphenylphosphineHCID 12642434HCID 12642434、化合物

生成物 1

HCID 10975591Benzene, (3-methyl-3-buten-1-ynyl)-

試薬・触媒・溶媒 2

HCID 5943Carbon Tetrachloride溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of 100 mmol of 2-methyl-4-phenylbut-1-en-3-ol (16.02 g) in 90 mL of tetrahydrofuran and 210 mL of carbon tetrachloride was mixed with 300 mmol (78.70 g) of dry triphenylphosphine. The solution was heated to boiling under reflux for 2 hours, whereupon a precipitate formed. After cooling, 400 mL of pentane was added and the precipitate was separated by filtration. The solvent was removed from the filtrate under reduced pressure and the residue was fractionally distilled to give 2-methyl-4-phenylbut-1-en-3-yne havng the formula: ##STR27##

後処理

  1. temperatureThe solution was heated
  2. temperatureunder reflux for 2 hours, whereupon a precipitate
  3. customformed
  4. temperatureAfter cooling
  5. customthe precipitate was separated by filtration
  6. customThe solvent was removed from the filtrate under reduced pressure
  7. distillationthe residue was fractionally distilled

出典と根拠

ORDレコード
ord-85373a38077f4b0893a500addc8f35e1
出典データセット
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06136940

反応ノート

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