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 Carbonate → 2-tert-Butyl-9,10-di(naphth-2-yl)anthracene

HRID 1438093
ノート
印刷プレビュー

反応式

HRID 1438093 の反応式
[C:1]([C:5]1[CH:18]=[CH:17][C:16]2[C:7](=[CH:8][C:9]3[C:14]([CH:15]=2)=[CH:13][CH:12]=[CH:11][CH:10]=3)[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].BrNC(=O)CCC(N)=O.C(C1C=C[C:43]2[C:34](=[C:35](Br)[C:36]3[C:41]([C:42]=2Br)=[CH:40][CH:39]=[CH:38][CH:37]=3)C=1)(C)(C)C.[CH:48]1[C:57]2[C:52](=[CH:53][CH:54]=[CH:55][CH:56]=2)[CH:51]=[CH:50][C:49]=1B(O)O.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O.C(O)C.C1(C)C=CC=CC=1.O>[CH3:3][C:1]([C:5]1[CH:18]=[CH:17][C:16]2[C:7](=[C:8]([C:43]3[CH:34]=[CH:35][C:36]4[C:41](=[CH:40][CH:39]=[CH:38][CH:37]=4)[CH:42]=3)[C:9]3[C:14]([C:15]=2[C:50]2[CH:49]=[CH:48][C:57]4[C:52](=[CH:53][CH:54]=[CH:55][CH:56]=4)[CH:51]=2)=[CH:13][CH:12]=[CH:11][CH:10]=3)[CH:6]=1)([CH3:4])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

10

反応物 5

HCID 11430Potassium CarbonateHCID 878002-tert-ButylanthraceneHCID 2734375(Naphthalen-2-yl)boronic acidHCID 41266102-Tert-butyl-9,10-dibromoanthraceneHCID 9834204N-Bromosuccinamide

生成物 1

HCID 218960962-tert-Butyl-9,10-di(naphth-2-yl)anthracene

試薬・触媒・溶媒

4
HCID 702Ethanol溶媒HCID 962Water溶媒HCID 1140Toluene溶媒HCID 6228Dimethylformamide溶媒2 回

実験手順

The 2-(t-butyl)anthracene (6.11g, 26.07 mmol) was placed into a 250 mL round bottom flask and was dissolved in dimethylformamide (80 mL) and was cooled on an ice bath. The N-bromosuccinamide (9.28g, 52.15 mmol) was dissolved in dimethylformamide (20 mL) and was added slowly to the reaction. After addition, the reaction was allowed to come to room temperature and was stirred for 3 hours. The mixture was poured into water (500 mL) and the solid collected, washed with water and then methanol. The product was collected, dried and then used directly in the next step. The 2-(t-butyl)-9,10-dibromoanthracene (9.8g, 24.99 mmol) was placed into a 250 mL round bottom flask along with 2-naphthylboronic acid (9.46g, 54.98 mmol), toluene (100 mL), ethanol (10 mL) and 2.0 aqueous potassium carbonate (75 mL). The reaction was purged with argon for 15 minutes and then Pd(PPh3)4 (0.29g) was added. The reaction was heated at reflux for 16 hours. The reaction was cooled and the organic layer was collected and washed with aqueous 5% HCI and then saturated aqueous brine solution. The organic layer was collected, dried and concentrated under reduced pressure. The compound was purified by flash chromatography with hexane and then dichloromethane which eluted the compound. Further purification was achieved by sublimation at 320° C. to give >99% purity of TBADN. This compound and its structure were confirmed by proton NMR analysis.

後処理

  1. temperaturewas cooled on an ice bath
  2. additionwas added slowly to the reaction
  3. additionAfter addition
  4. customto come to room temperature
  5. customthe solid collected
  6. washwashed with water
  7. customThe product was collected
  8. customdried
  9. customThe reaction was purged with argon for 15 minutes
  10. additionPd(PPh3)4 (0.29g) was added
  11. temperatureThe reaction was heated
  12. temperatureat reflux for 16 hours
  13. temperatureThe reaction was cooled
  14. customthe organic layer was collected
  15. washwashed with aqueous 5% HCI
  16. customThe organic layer was collected
  17. customdried
  18. concentrationconcentrated under reduced pressure
  19. customThe compound was purified by flash chromatography with hexane
  20. washdichloromethane which eluted the compound
  21. customFurther purification
  22. customwas achieved by sublimation at 320° C.

出典と根拠

ORDレコード
ord-5166093cebc94fc6848ebe07577ed398
出典データセット
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07622619B2

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