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

Potassium tert-butoxide → 2-{2-Chloro-4-fluoro-3-[prop-1-en-1-yl]phenyl}-1,3-dioxolane

HRID 2046644
ノート
印刷プレビュー

反応式

HRID 2046644 の反応式
[CH3:1][C:2](C)([O-])C.[K+].[Cl:7][C:8]1[C:15]([CH:16]2[O:20][CH2:19][CH2:18][O:17]2)=[CH:14][CH:13]=[C:12]([F:21])[C:9]=1[CH:10]=O>[Br-].C([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)C.O1CCCC1.[Cl-].[Na+].O>[Cl:7][C:8]1[C:9]([CH:10]=[CH:1][CH3:2])=[C:12]([F:21])[CH:13]=[CH:14][C:15]=1[CH:16]1[O:20][CH2:19][CH2:18][O:17]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 2

HCID 23665647Potassium tert-butoxideHCID 593705312-Chloro-3-(1,3-dioxolan-2-yl)-6-fluorobenzaldehyde

生成物 1

HCID 686033642-{2-Chloro-4-fluoro-3-[prop-1-en-1-yl]phenyl}-1,3-dioxolane収率 99.3%

試薬・触媒・溶媒 3

HCID 73727Phosphonium, ethyltriphenyl-, bromide (1:1)触媒HCID 8028Tetrahydrofuran溶媒
HCID 57417360
Sodium chloride; water
溶媒

実験手順

To a solution of ethyltriphenylphosphonium bromide (3.43 g) in tetrahydrofuran (15 mL) was added potassium tert-butoxide (1.31 g) at 0° C., and the mixture was stirred at room temperature for 1 hr. Successively, 2-chloro-3-(1,3-dioxolan-2-yl)-6-fluorobenzaldehyde (1.35 g) was added to the mixture, and the mixture was stirred for 2.5 hr. To the reaction mixture was added saturated brine, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give crude 2-{2-chloro-4-fluoro-3-[prop-1-en-1-yl]phenyl}-1,3-dioxolane (1.41 g).

後処理

  1. stirringthe mixture was stirred for 2.5 hr
  2. extractionthe mixture was extracted with ethyl acetate
  3. dry with materialThe extract was dried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-463dbc2f9daa41daaa87b48956d18432
出典データセット
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08592452B2

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