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Sodium Hydroxide → 3-(Methanesulfonylmethyl)aniline

HRID 514694
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HRID 514694 반응식
[CH3:1][S:2]([CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-])=O)[CH:7]=1)(=[O:4])=[O:3].[OH-].[Na+]>Cl.C1COCC1.[Cl-].[Ti+3].[Cl-].[Cl-]>[CH3:1][S:2]([CH2:5][C:6]1[CH:7]=[C:8]([CH:9]=[CH:10][CH:11]=1)[NH2:12])(=[O:3])=[O:4]
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참가 물질

6

반응물 2

HCID 14798Sodium HydroxideHCID 179084331-(Methanesulfonylmethyl)-3-nitrobenzene

생성물 1

HCID 219563393-(Methanesulfonylmethyl)aniline수율 102.1%

시약·촉매·용매 3

HCID 10313229titanium(III) trichloride촉매HCID 313Hydrochloric Acid용매HCID 8028
Tetrahydrofuran
용매

실험 절차

Titanium(III)chloride solution (about 15%) in about 10% hydrochloric acid (162 mL; Merck Schuchardt OHG) was added to a stirred solution of 1-[(methylsulfonyl)methyl]-3-nitrobenzene (5.1 g; 23.8 mmol) in THF (250 mL) at room temperature and the batch was stirred for 16 hours. By adding 1N sodium hydroxide solution the pH value of the reaction mixture was raised to 10 before the batch was extracted with ethyl acetate (2×). The combined organic phases were washed with brine, filtered using a Whatman filter and concentrated to give the desired product (4.5 g) that was used without further purification.

후처리

  1. temperaturewas raised to 10 before the batch
  2. extractionwas extracted with ethyl acetate (2×)
  3. washThe combined organic phases were washed with brine
  4. filtrationfiltered
  5. filtrationfilter
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-55a767625104494a81a623826cd4e827
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09108926B2

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