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

Calcium Carbonate → Benzaldehyde, 3-(4-fluorophenoxy)-

HRID 704816
ノート
印刷プレビュー

反応式

HRID 704816 の反応式
Br[CH:2](Br)[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][C:10]2[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=2)[CH:4]=1.C(=O)([O-])[O-:19].[Ca+2]>C(O)C.O>[F:16][C:13]1[CH:14]=[CH:15][C:10]([O:9][C:5]2[CH:4]=[C:3]([CH:8]=[CH:7][CH:6]=2)[CH:2]=[O:19])=[CH:11][CH:12]=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 2

HCID 10112Calcium CarbonateHCID 20073369HCID 20073369、化合物

生成物 1

HCID 3085320Benzaldehyde, 3-(4-fluorophenoxy)-収率 92.4%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

A solution of the product of step (b) (16.04 g) in a mixture of ethanol (100 ml) and water (25 ml) was treated with precipitated calcium carbonate (13.37 g) and the mixture refluxed for 20 hours. After cooling, the mixture was filtered, the filtrate stripped, and the residue taken up in 2 M aqu. HCl (100 ml) and extracted with ether (200 ml). The extract was washed with water (100 ml), dried over Na2SO4 and stripped to give a pale yellow oil which was distilled under reduced pressure to give the desired product (8.90 g), bp 100°-130° C./0.2 mm Hg.

後処理

  1. temperaturethe mixture refluxed for 20 hours
  2. temperatureAfter cooling
  3. filtrationthe mixture was filtered
  4. extractionHCl (100 ml) and extracted with ether (200 ml)
  5. washThe extract was washed with water (100 ml)
  6. dry with materialdried over Na2SO4
  7. customto give a pale yellow oil which
  8. distillationwas distilled under reduced pressure

出典と根拠

ORDレコード
ord-8ee1f8debc9d451f9013b77fecc83891
出典データセット
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04988733

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