1,3,5-Trimethyl-4-nitro-1H-pyrazole → 1,3,5-trimethyl-1H-pyrazol-4-amine

HRID 264057

反応式

HRID 264057 の反応式
[N+:1]([C:4]1[C:5]([CH3:11])=[N:6][N:7]([CH3:10])[C:8]=1[CH3:9])([O-])=O>[Ni].N>[NH2:1][C:4]1[C:5]([CH3:11])=[N:6][N:7]([CH3:10])[C:8]=1[CH3:9]

参加物

4

反応物 1

HCID 1210191,3,5-Trimethyl-4-nitro-1H-pyrazole

生成物 1

HCID 1616031,3,5-trimethyl-1H-pyrazol-4-amine

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 222Ammonia溶媒

実験手順

The compounds from (b) above (2.3 g; 0.014 moles) was catalytically hydrogenated using Raney nickel (1 g) in methanolic ammonia (100 mL) under a hydrogen atmosphere at 50 psi. The catalyst was filtered and the solution concentrated in vacuo, leaving a residue that was triturated several times with ethyl ether. The decanted solvent was concentrated to dryness, leaving a pale red solid. Yield: 1.3 g (70%). 1H NMR (CDCl3) δ3.6 (s, 3H), 2.4 (bs, 2H), 2.1 (s, 6H) ppm.

後処理

  1. filtrationThe catalyst was filtered
  2. concentrationthe solution concentrated in vacuo
  3. customleaving a residue that
  4. customwas triturated several times with ethyl ether
  5. concentrationThe decanted solvent was concentrated to dryness
  6. customleaving a pale red solid

出典と根拠

ORDレコード
ord-682b3310c3b4493d8dfc6e2a319a3bb6
出典データセット
uspto-grants-1997_07
特許番号
US05646170

関連ノート

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