ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Water → 1-Vinyl-4-ethyl-2,6,7-trioxabicyclo[2,2,2] octane

HRID 2295528
ノート
印刷プレビュー

反応式

HRID 2295528 の反応式
Br[CH:2]([C:4]12[O:11][CH2:10][C:7]([CH2:12][CH3:13])([CH2:8][O:9]1)[CH2:6][O:5]2)[CH3:3].CC(C)([O-])C.[K+].O>O1CCCC1>[CH:2]([C:4]12[O:5][CH2:6][C:7]([CH2:12][CH3:13])([CH2:8][O:9]1)[CH2:10][O:11]2)=[CH2:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 204748331-(1-Bromoethyl)-4-ethyl-2,6,7-trioxabicyclo[2.2.2]octaneHCID 23665647Potassium tert-butoxide

生成物 1

HCID 136431181-Vinyl-4-ethyl-2,6,7-trioxabicyclo[2,2,2] octane収率 83%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

25 g (0.1 moles) of the product obtained in step (b) above was added dropwise over about one hour at room temperature to a solution of 11 g (0.1 moles) of potassium t-butoxide in 100 ml of tetrahydrofuran placed in a 250 ml flask. The mixture was heated at reflux temperature for 5 hours and the reaction solution obtained was poured into water. The resulting solution was extracted with ethyl ether and the organic layer was dried over anhydrous magnesium sulfate and concentrated by evaporation of the ether. The residue was distilled under reduced pressure to give 14 g (83%) of the title compound with a boiling point of 68°-72° C./2 mmHg and a specific gravity of 1.216 (Method D).

後処理

  1. customplaced in a 250 ml flask
  2. temperatureThe mixture was heated
  3. temperatureat reflux temperature for 5 hours
  4. customthe reaction solution obtained
  5. extractionThe resulting solution was extracted with ethyl ether
  6. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  7. concentrationconcentrated by evaporation of the ether
  8. distillationThe residue was distilled under reduced pressure

出典と根拠

ORDレコード
ord-ecbeaa48e4b5451d9e52edf1263ad5fb
出典データセット
uspto-grants-1984_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04425473

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート