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

Dimethyl 2,2'-(1,3-dioxolane-2,2-diyl)diacetate → 2-(2-(2-Hydroxyethyl)-1,3-dioxolan-2-yl)ethan-1-ol

HRID 1015973
ノート
印刷プレビュー

反応式

HRID 1015973 の反応式
[O:1]1[CH2:5][CH2:4][O:3][C:2]1([CH2:11][C:12](OC)=[O:13])[CH2:6][C:7](OC)=[O:8].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[O:1]1[CH2:5][CH2:4][O:3][C:2]1([CH2:6][CH2:7][OH:8])[CH2:11][CH2:12][OH:13]
参加物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 228900Dimethyl 2,2'-(1,3-dioxolane-2,2-diyl)diacetateHCID 21226445Aluminium lithium hydride

生成物 1

HCID 5760202-(2-(2-Hydroxyethyl)-1,3-dioxolan-2-yl)ethan-1-ol収率 66.7%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 2.6 g (12 mmol) of dimethyl 2,2′-(1,3-dioxolane-2,2-diyl)diacetate in 100 mL of dry THF was added 1.4 g (36 mmol) of LAH at 0° C. The reaction mixture was then refluxed for 1 h, was quenched with 15% NaOH aqueous solution (3 mL) and water (3 mL). The mixture was stirred overnight, filtered through celite. The residue was washed twice with THF (100 mL×2). The combined organic phase was evaporated. Chromatography on silica gel afforded 1.3 g (8.0 mmol, yield: 66%) of 2,2′-(1,3-dioxolane-2,2-diyl)diethanol: MS (m/e): 163 (M+1)+.

後処理

  1. temperatureThe reaction mixture was then refluxed for 1 h
  2. customwas quenched with 15% NaOH aqueous solution (3 mL) and water (3 mL)
  3. filtrationfiltered through celite
  4. washThe residue was washed twice with THF (100 mL×2)
  5. customThe combined organic phase was evaporated

出典と根拠

ORDレコード
ord-2859ca561f724b74aa6217654c49820c
出典データセット
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07985730B2

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