N,N-Dimethylaniline → HCID 178482873、化合物

HRID 46417

反応式

HRID 46417 の反応式
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]2[NH:6][N:7]=[N:8][C:4]=2[CH:3]=1.Cl.CN([C:15]1[CH:23]=[CH:22][C:18](C(Cl)=O)=[C:17]([N:24]=[N:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:16]=1)C.[CH3:32][N:33]([CH3:40])C1C=CC=CC=1.[O:41]1CCC[CH2:42]1>>[NH:6]1[C:5]2[CH:9]=[CH:10][C:2]([NH:1][C:42](=[O:41])[C:29]3[CH:28]=[CH:27][C:26]([N:25]=[N:24][C:17]4[CH:16]=[CH:15][C:23]([N:33]([CH3:40])[CH3:32])=[CH:22][CH:18]=4)=[CH:31][CH:30]=3)=[CH:3][C:4]=2[N:8]=[N:7]1

参加物

5

反応物 4

HCID 949N,N-DimethylanilineHCID 8028TetrahydrofuranHCID 131711441HCID 131711441、化合物HCID 178507366HCID 178507366、化合物

生成物 1

HCID 178482873HCID 178482873、化合物

実験手順

A mixture of 5-aminobenzotriazole (0.47 g), 4-(N,N-dimethylamino)-phenylazobenzoyl chloride, hydrochloride (1.13 g) and N,N-dimethylaniline (0.84 g) in dry tetrahydrofuran was stirred overnight and the resulting precipitate was filtered off and recrystallized in a dimethylformamide/water mixture to give pure dye, 0.73 g, m.p. 246°, λmax (methanol)=435 nm.

後処理

  1. filtrationthe resulting precipitate was filtered off
  2. customrecrystallized in a dimethylformamide/water mixture
  3. customto give pure dye, 0.73 g, m.p. 246°, λmax (methanol)=435 nm

出典と根拠

ORDレコード
ord-fe14c8a2eb854e79aad88b5c6bd5ca41
出典データセット
uspto-grants-1979_11
特許番号
US04173478

関連ノート

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