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Hydrochloric Acid → Methyl N-(3-chloro-4-hydroxyphenyl)carbamate

HRID 1597801
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HRID 1597801 반응식
[OH-].[Na+].[NH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[C:6]([Cl:11])[CH:5]=1.Cl[C:13]([O:15][CH3:16])=[O:14].Cl>O>[Cl:11][C:6]1[CH:5]=[C:4]([NH:3][C:13](=[O:14])[O:15][CH3:16])[CH:9]=[CH:8][C:7]=1[OH:10]
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 6586Methyl chloroformateHCID 14798Sodium HydroxideHCID 775784-Amino-2-chlorophenol

생성물 1

HCID 18932212Methyl N-(3-chloro-4-hydroxyphenyl)carbamate수율 87%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

5 ml of water and 2.5 ml of 10% aqueous sodium hydroxide solution were carefully added to 1.70 g of 4-amino-2-chlorophenol cooled in an ice-water bath and 2 ml of methyl chloroformate were added dropwise to the resulting mixture. The reaction mixture was then stirred for 3 hours at room temperature, at the end of which it was acidified with 4 ml of 2N hydrochloric acid, and the resulting mixture was extracted with methylene; chloride. The resulting extract was washed with water and then dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure to give a crude crystalline solid which was purified by column chromatography through silica gel using a 2:1 by volume mixture of hexane and ethyl acetate as the eluent to give 2.08 g (yield 87%) of the title compound as a pale brown crystalline solid.

후처리

  1. temperaturecooled in an ice-water bath
  2. extractionthe resulting mixture was extracted with methylene
  3. extractionThe resulting extract
  4. washwas washed with water
  5. dry with materialdried over anhydrous sodium sulfate
  6. customThe solvent was then removed by evaporation under reduced pressure
  7. customto give a crude crystalline solid which
  8. customwas purified by column chromatography through silica gel using a 2:1
  9. additionby volume mixture of hexane and ethyl acetate as the eluent

출처 및 근거

ORD 기록
ord-2368dd68468a480ea51565699944a8cf
출처 데이터셋
uspto-grants-1998_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05736487

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