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

1-Naphthaldehyde → 37630-26-5

HRID 1635945
ノート
印刷プレビュー

反応式

HRID 1635945 の反応式
[C:1]1([CH:11]=O)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.C([O-])(=O)C.[NH4+].[N+:18]([CH3:21])([O-:20])=[O:19].C(OC(=O)C)C>CCCCCC>[N+:18](/[CH:21]=[CH:11]/[C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1)([O-:20])=[O:19]
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 61951-NaphthaldehydeHCID 6375NitromethaneHCID 8857Ethyl AcetateHCID 517165Ammonium Acetate

生成物 1

HCID 538167937630-26-5収率 62%

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

実験手順

7.81 g (50 mmol) of 1-naphthaldehyde and 1.54 g (20 mmol) of ammonium acetate were added to 70 ml of nitromethane and heated under reflux for 3 hours (see: J. Org. Chem., 1984, 49, 4761). 100 ml of ethylacetate was added and the resulting mixture was washed with 50 ml of water and 50 ml of brine. The organic layer was collected and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the residue was subjected to column chromatography (eluent: hexane/ethylacete=90/10, v/v) to give 6.27 g( 0.031 mmol, Yield 62%) of the title compound.

後処理

  1. temperatureheated
  2. temperatureunder reflux for 3 hours (see: J. Org. Chem., 1984, 49, 4761)
  3. washthe resulting mixture was washed with 50 ml of water and 50 ml of brine
  4. customThe organic layer was collected
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customThe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-536971e4e6074feaa6d8340e274fbb76
出典データセット
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06511978B1

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