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Water → HCID 17750755、化合物

HRID 1270732
ノート
印刷プレビュー

反応式

HRID 1270732 の反応式
COC(=O)[NH:4][C:5]1[C:10]([F:11])=[C:9]([CH3:12])[CH:8]=[CH:7][C:6]=1[Cl:13].O.[OH-].[Na+]>CO>[Cl:13][C:6]1[CH:7]=[CH:8][C:9]([CH3:12])=[C:10]([F:11])[C:5]=1[NH2:4]
参加物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 962WaterHCID 14798Sodium HydroxideHCID 68802629HCID 68802629、化合物

生成物 1

HCID 17750755HCID 17750755、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

N-(2-chloro-5-methyl-6-fluorophenyl)-carbamic acid methyl ester (39 g, 0.18 mmol) is dissolved in MeOH (150 mL), water (150 mL) and 30% NaOH solution (150 mL). The reaction mixture is heated to reflux temperature for 3 days and then cooled to room temperature. The reaction is concentrated by rotary evaporator to remove most of the methanol and then partitioned between Et2O (500 mL) and water (500 mL). The aqueous phase is extracted again with Et2O (250 mL) and the combined organic layers washed with brine (500 mL), dried and concentrated by rotary evaporator. The crude product is purified by bulb-to-bulb distillation to give 2-chloro-5-methyl-6-fluoroaniline as a colorless oil (b.p. 120–131° C. at ˜20 mm of Hg), which forms a white crystalline solid upon storage at 4° C.

後処理

  1. temperatureThe reaction mixture is heated
  2. temperatureto reflux temperature for 3 days
  3. concentrationThe reaction is concentrated by rotary evaporator
  4. customto remove most of the methanol
  5. custompartitioned between Et2O (500 mL) and water (500 mL)
  6. extractionThe aqueous phase is extracted again with Et2O (250 mL)
  7. washthe combined organic layers washed with brine (500 mL)
  8. customdried
  9. concentrationconcentrated by rotary evaporator
  10. distillationThe crude product is purified by bulb-to-bulb distillation

出典と根拠

ORDレコード
ord-c06e3833c2ea42ed953131ef998c9ad2
出典データセット
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07202364B2

反応ノート

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