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Sodium, 2,4-cyclopentadien-1-yl- → 2-methoxyethylcyclopentadiene

HRID 2395215
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HRID 2395215 반응식
[CH3:1][O:2][CH2:3][CH2:4]OS(C1C=CC(C)=CC=1)(=O)=O.[CH-:16]1[CH:20]=[CH:19][CH:18]=[CH:17]1.[Na+]>C1COCC1>[CH3:1][O:2][CH2:3][CH2:4][C:16]1[CH2:20][CH:19]=[CH:18][CH:17]=1
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참가 물질

4

반응물 2

HCID 78681Sodium, 2,4-cyclopentadien-1-yl-HCID 86977Ethanol, 2-methoxy-, 1-(4-methylbenzenesulfonate)

생성물 1

HCID 108968552-methoxyethylcyclopentadiene수율 44%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

To a solution of 19.7 g(85.7 mmol) 2-methoxyethyltosylate as prepared in step (a) in 200 ml THF cooled to 0° C. was added 55 ml of 2.0M (110 mmol) sodium cyclopentadienylide in THF. The reaction mixture was allowed to warm to room temperature and was stirred for 16 h. 100 ml concentrated aqueous saline solution was added and the product extracted with diethyl ether (3×75 ml). The combined organic fractions were dried over sodium sulphate for 16 hrs, filtered and the solvents removed under reduced pressure using a rotary evaporator to yield a brown oil. The crude product was distilled under reduced pressure (b.p. 40-°44° C. at 2-3 mm Hg) to give 4.5 g of a colourless oil (37.7 mmol, 44.0%).

후처리

  1. temperatureto warm to room temperature
  2. extractionthe product extracted with diethyl ether (3×75 ml)
  3. dry with materialThe combined organic fractions were dried over sodium sulphate for 16 hrs
  4. filtrationfiltered
  5. customthe solvents removed under reduced pressure
  6. customa rotary evaporator
  7. customto yield a brown oil
  8. distillationThe crude product was distilled under reduced pressure (b.p. 40-°44° C. at 2-3 mm Hg)

출처 및 근거

ORD 기록
ord-a1dcaa9a7c2f4220b9fc328da916f347
출처 데이터셋
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05814574

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