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Cyclopentanol → HCID 10859381、化合物

HRID 1788881
ノート
印刷プレビュー

反応式

HRID 1788881 の反応式
[CH:1]1([OH:6])[CH2:5][CH2:4][CH2:3][CH2:2]1.[Na].O1CCCC1.[Cl:13][C:14]1[C:18]([F:20])([F:19])[C:17]([F:22])([F:21])[C:16]([F:24])([F:23])[C:15]=1Cl>CCOCC>[CH:1]1([O:6][C:15]2[C:16]([F:24])([F:23])[C:17]([F:21])([F:22])[C:18]([F:19])([F:20])[C:14]=2[Cl:13])[CH2:5][CH2:4][CH2:3][CH2:2]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 4

HCID 7298CyclopentanolHCID 8028TetrahydrofuranHCID 128151,2-DichloroperfluorocyclopenteneHCID 5360545Sodium

生成物 1

HCID 10859381HCID 10859381、化合物収率 79%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

Cyclopentanol (23 g, 0.27 mol) and sodium metal (5.6 g, 0.24 mol) were refluxed with 25 ml dry tetrahydrofuran (THF) overnight. The reaction mixture was diluted with 200 ml of dry ether and then added to 1,2-dichlorohexafluorocyclopentene (49 g, 0.2 mol) in 100 ml of dry ether at room temperature with stirring over 20 minutes. After the completion of the addition, the reaction mixture was heated to reflux for 2 hours. The reaction mixture was poured into ice water (150 ml) and the organic layer was separated. Then the aqueous layer was extracted with 4 portions of 100 ml of ether. Next, the organic layer and the ether extracts were combined and dried over CaCl2 overnight. Thereafter, the solvent was distilled out at atmospheric pressure. That which remained was distilled under reduced pressure to give the desired 2-chlorohexafluorocyclopentenyl cyclopentyl ether in 79% yield based on the 1,2-dichlorohexafluorocyclopentene used.

後処理

  1. additionAfter the completion of the addition
  2. temperaturethe reaction mixture was heated
  3. temperatureto reflux for 2 hours
  4. customthe organic layer was separated
  5. extractionThen the aqueous layer was extracted with 4 portions of 100 ml of ether
  6. dry with materialdried over CaCl2 overnight
  7. distillationThereafter, the solvent was distilled out at atmospheric pressure
  8. distillationThat which remained was distilled under reduced pressure

出典と根拠

ORDレコード
ord-bf696a9a0941417da664285712a10733
出典データセット
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04686024

反応ノート

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