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Water → HCID 17750755, 화합물

HRID 1270732
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HRID 1270732 반응식
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]
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참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 68802629HCID 68802629, 화합물

생성물 1

HCID 17750755HCID 17750755, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-c06e3833c2ea42ed953131ef998c9ad2
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07202364B2

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