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

HRID 2395215
ノート
印刷プレビュー

反応式

HRID 2395215 の反応式
[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
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

4

反応物 2

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

生成物 1

HCID 108968552-methoxyethylcyclopentadiene収率 44%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

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%).

後処理

  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)

出典と根拠

ORDレコード
ord-a1dcaa9a7c2f4220b9fc328da916f347
出典データセット
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05814574

反応ノート

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