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Dimethylamine → HCID 21473553、化合物

HRID 2294136
ノート
印刷プレビュー

反応式

HRID 2294136 の反応式
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([N+:11]([O-:13])=[O:12])=[C:6]([CH:10]=1)[C:7](O)=[O:8].C(Cl)(=O)C(Cl)=O.[CH3:20][NH:21][CH3:22].[OH-].[Na+]>C(Cl)Cl.O1CCOCC1.O>[CH3:20][N:21]([CH3:22])[C:7](=[O:8])[C:6]1[CH:10]=[C:2]([CH3:1])[CH:3]=[CH:4][C:5]=1[N+:11]([O-:13])=[O:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 674DimethylamineHCID 14798Sodium HydroxideHCID 183715-Methyl-2-nitrobenzoic acidHCID 65578Oxalyl chloride

生成物 1

HCID 21473553HCID 21473553、化合物収率 95.7%

試薬・触媒・溶媒 3

HCID 962Water溶媒
HCID 6344
Dichloromethane
溶媒
HCID 312751,4-Dioxane溶媒

実験手順

A mixture of 5-methyl-2-nitrobenzoic acid (10 g, 55.2 mmol) and oxalyl chloride (6 mL, 68.8 mmol) in 100 mL of methylene chloride was stirred under argon at room temperature for 2 hours. The mixture was concentrated and the residue was co-evaporated twice with toluene. The residue was dissolved in 60 mL of dioxane and the solution was added dropwise to a mixture of aqueous dimethylamine (8.2 g, 40% w/w, 72.7 mmol) and sodium hydroxide (2.2 g, 55 mmol) in 20 mL of dioxane at 0° C. The mixture was stirred at room temperature for 1 hour and then poured into water. The mixture was extracted with ethyl acetate (2×150 mL), dried (Na2SO4), filtered and concentrated to give N,N,5-trimethyl-2-nitrobenzamide (11 g, 52.8 mmol).

後処理

  1. concentrationThe mixture was concentrated
  2. dissolutionThe residue was dissolved in 60 mL of dioxane
  3. stirringThe mixture was stirred at room temperature for 1 hour
  4. extractionThe mixture was extracted with ethyl acetate (2×150 mL)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-ec0b54d5cda246359004f35953e8e89e
出典データセット
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05688795

反応ノート

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