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

(Methoxymethylene)triphenylphosphorane → HCID 131734415、化合物

HRID 587857
ノート
印刷プレビュー

反応式

HRID 587857 の反応式
[CH3:1][O:2][CH:3]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.CC(C)([O-])C.[K+].[C:29]12([O:44][CH2:43][CH2:42][O:41]1)[C:38]1[C:33](=[CH:34][CH:35]=[CH:36][CH:37]=1)[CH2:32][C@@H:31]([CH:39]=O)[CH2:30]2>O1CCCC1>[CH3:1][O:2][CH:3]=[CH:39][C@@H:31]1[CH2:32][C:33]2[C:38](=[CH:37][CH:36]=[CH:35][CH:34]=2)[C:29]2([O:44][CH2:43][CH2:42][O:41]2)[CH2:30]1
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 11748776(Methoxymethylene)triphenylphosphoraneHCID 23665647Potassium tert-butoxideHCID 118324708HCID 118324708、化合物

生成物 1

HCID 131734415HCID 131734415、化合物収率 78%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒3 回

実験手順

To a stirred solution of (methoxymethylene)triphenylphosphorane (6.74 g, 21.99 mmol) in tetrahydrofuran (30 mL) was added drop-wise a solution of potassium tert-butoxide (3.08 g, 27.5 mmol) in THF at −30° C. under argon, and the mixture was stirred for 30 min. Then a solution of (R)-3′,4′-dihydro-2′H-spiro[[1,3]dioxolane-2,1′-naphthalene]-3′-carbaldehyde (4.0 g, 18.33 mmol) in THF was added drop-wise and reaction was stirred for 1 h at −30° C. Reaction was monitored by TLC. Reaction mixture quenched with water at −30° C. and allowed to RT, diluted with water (25 mL) and extracted with ethyl acetate (2×50 mL), dried over Na2SO4, filtered and concentrated to give crude product (8 g). The crude compound was purified with silica gel flash column chromatography (Biotage) to give (R)-3′-(2-methoxyvinyl)-3′,4′-dihydro-2′H-spiro[[1,3]dioxolane-2,1′-naphthalene] (3.5 g, 14.21 mmol, 78% yield) as colourless liquid; m/z 246.6.

後処理

  1. customdrop-wise and reaction
  2. stirringwas stirred for 1 h at −30° C
  3. customReaction
  4. customReaction mixture
  5. customquenched with water at −30° C.
  6. customallowed to RT
  7. additiondiluted with water (25 mL)
  8. extractionextracted with ethyl acetate (2×50 mL)
  9. dry with materialdried over Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated
  12. customto give crude product (8 g)
  13. customThe crude compound was purified with silica gel flash column chromatography (Biotage)

出典と根拠

ORDレコード
ord-674dc801d3394626bcb1aeabf21294f9
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09227919B2

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