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

HRID 369442
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HRID 369442 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8003PentaneHCID 11776TriphenylphosphineHCID 12642434HCID 12642434, 화합물

생성물 1

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

시약·촉매·용매 2

HCID 5943Carbon Tetrachloride용매HCID 8028Tetrahydrofuran용매

실험 절차

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##

후처리

  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

출처 및 근거

ORD 기록
ord-85373a38077f4b0893a500addc8f35e1
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06136940

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