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

Diethyl Ether → 3,3-Difluoro-4-methylpentane-1,4-diol

HRID 745636
ノート
印刷プレビュー

反応式

HRID 745636 の反応式
[CH3:1][Li].[F:3][C:4]([F:13])([CH2:10][CH2:11][OH:12])C(OCC)=O.CC[O:16][CH2:17][CH3:18]>>[CH3:1][C:17]([OH:16])([CH3:18])[C:4]([F:13])([F:3])[CH2:10][CH2:11][OH:12]
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 3

HCID 3283Diethyl EtherHCID 13189245Ethyl 2,2-difluoro-4-hydroxybutanoateHCID 178418348HCID 178418348、化合物

生成物 1

HCID 131892463,3-Difluoro-4-methylpentane-1,4-diol

反応条件

温度
25 °C

実験手順

To a solution of 311 mL of 1.6M ethereal methyllithium (0.498 mol) of 0° was added dropwise 11.16 g (0.066 mol) of ethyl 2,2-difluoro-4-hydroxybutanoate in 150 mL of ether. The mixture was stirred at 0° C. for 1 hr and at 25° C. for 17 hr. The mixture was quenched by adding 14 mL of saturated brine at 0° C. The mixture was poured into saturated brine and the product was isolated with ether. The ether layers were dried over anhydrous magnesium sulfate, filtered, and evaporated to dryness. The residue was chromatographed on 0.06-0.20 mm of silica gel to give 4-methyl-3,3-difluoro-1,4-pentanediol.

後処理

  1. customThe mixture was quenched
  2. additionby adding 14 mL of saturated brine at 0° C
  3. additionThe mixture was poured into saturated brine
  4. customthe product was isolated with ether
  5. dry with materialThe ether layers were dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customevaporated to dryness
  8. customThe residue was chromatographed on 0.06-0.20 mm of silica gel

出典と根拠

ORDレコード
ord-8480cec98dc64fe2ae1e34f4a09358a3
出典データセット
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04599330

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート