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

Tetrahydrofuran → 2-[8-(4-Chlorophenoxy)octyl]-5,6-dimethoxyindan-4,7-dione

HRID 2268531
ノート
印刷プレビュー

反応式

HRID 2268531 の反応式
[Cl:1][C:2]1[CH:33]=[CH:32][C:5]([O:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH:15]2[CH2:23][C:22]3[C:17](=[C:18]([O:30]C)[C:19]([O:28][CH3:29])=[C:20]([O:26][CH3:27])[C:21]=3[O:24]C)[CH2:16]2)=[CH:4][CH:3]=1.N1C(C(O)=O)=CC=CC=1C(O)=O.C1COCC1.O=[N+]([O-])[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[Ce+4].[NH4+].[NH4+]>O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH:15]2[CH2:16][C:17]3[C:18](=[O:30])[C:19]([O:28][CH3:29])=[C:20]([O:26][CH3:27])[C:21](=[O:24])[C:22]=3[CH2:23]2)=[CH:32][CH:33]=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 4

HCID 8028TetrahydrofuranHCID 103672,6-Pyridinedicarboxylic acidHCID 180504Ceric ammonium nitrateHCID 183485992-[8-(4-Chlorophenoxy)octyl]-4,5,6,7-tetramethoxyindan

生成物 1

HCID 98248512-[8-(4-Chlorophenoxy)octyl]-5,6-dimethoxyindan-4,7-dione収率 50.5%

試薬・触媒・溶媒 1

HCID 962
Water
溶媒
3 回

実験手順

To a mixture of 2-[8-(4-chlorophenoxy)octyl]-4,5,6,7-tetramethoxyindan (676 mg), 2,6-pyridinedicarboxylic acid (712 mg), THF (14 ml), and water (7 ml) was dropwise added a solution of CAN (3.11 g) in water (7 ml) with cooling with ice. After the reaction mixture was stirred for 15 min, water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride and dried. The solvent was removed in vacuo. The residue was purified by silica gel column chromatography (hexane to hexane:ethyl acetate=10:1) and then with recrystallization from hexane-diethyl ether to yield the entitled compound (320 mg) as crystals.

後処理

  1. temperaturewith cooling with ice
  2. extractionwas extracted with ethyl acetate
  3. washThe organic layer was washed with water and saturated aqueous sodium chloride
  4. customdried
  5. customThe solvent was removed in vacuo
  6. customThe residue was purified by silica gel column chromatography (hexane to hexane:ethyl acetate=10:1)
  7. customwith recrystallization from hexane-diethyl ether

出典と根拠

ORDレコード
ord-bc1e6bd238f44327957a68420c5eca30
出典データセット
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06326369B1

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