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2-Iodoaniline → (2-Iodophenyl)hydrazine

HRID 589345
ノート
印刷プレビュー

反応式

HRID 589345 の反応式
[I:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH2:8].[N:9]([O-])=O.[Na+].O.O.Cl[Sn]Cl>Cl>[I:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][NH2:9]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 119952-IodoanilineHCID 61436Stannous chloride dihydrateHCID 23668193Sodium Nitrite

生成物 1

HCID 1381941(2-Iodophenyl)hydrazine収率 44%

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

反応条件

温度
0 °C

実験手順

21.9 g (100 mmol) o-iodophenyl amine was dissolved in 40 mL concentrated hydrochloric acid. At 0° C., 6.9 g (100 mmol) sodium nitrite (dissolved in 35 mL water) was added dropwise, and stirred at 0° C. for half an hour. Then, SnCl2.2H2O 64.7 g (300 mmol) (dissolved in 70 mL concentrated hydrochloric acid) was added dropwise slowly, and reacted for about 3 h until complete. It was filtered to obtain a white solid, washed with a saturated solution of sodium chloride, and then washed with a mixed solvent of petroleum ether and diethyl ether (1:1). Then, the solid was adjusted to be basic with sodium hydroxide solution. The solid impurity therein was filtered, the aqueous phase was extracted with dichloromethane several times, the organic phases combined, dried, rotate evaporated to dryness to obtain a colorless oil 10.3 g, at a yield of 44.0%.

後処理

  1. customreacted for about 3 h until complete
  2. filtrationIt was filtered
  3. customto obtain a white solid
  4. washwashed with a saturated solution of sodium chloride
  5. washwashed with a mixed solvent of petroleum ether and diethyl ether (1:1)
  6. filtrationThe solid impurity therein was filtered
  7. extractionthe aqueous phase was extracted with dichloromethane several times
  8. customdried
  9. customrotate evaporated to dryness

出典と根拠

ORDレコード
ord-ba65a172163c42eb8567bf2271d00387
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09233098B2

反応ノート

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