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Sodium hydrosulfide → Methyl 4-mercapto-2-methyl-5-nitrobenzoate

HRID 1942491
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HRID 1942491 반응식
Cl[C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[C:4]([CH3:15])[CH:3]=1.[SH-:16].[Na+]>CO>[SH:16][C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[C:4]([CH3:15])[CH:3]=1
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참가 물질

4

반응물 2

HCID 28015Sodium hydrosulfideHCID 10633188Methyl 4-chloro-2-methyl-5-nitrobenzoate

생성물 1

HCID 58376194Methyl 4-mercapto-2-methyl-5-nitrobenzoate수율 97.7%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of methyl 4-chloro-2-methyl-5-nitrobenzoate (1.21 g) in methanol (20 ml) was added sodium hydrosulfide (561 mg), and the mixture was refluxed with stirring for 2 hours. After the reaction was complete, the reaction solution was concentrated, and methanol was concentrated under reduced pressure. Then, to the resultant were added water and 2N hydrochloric acid, and the mixture was extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered, concentrated under reduced pressure. The obtained residue was purified by column chromatography to give the title compound (1.17 g).

후처리

  1. temperaturethe mixture was refluxed
  2. concentrationthe reaction solution was concentrated
  3. concentrationmethanol was concentrated under reduced pressure
  4. additionThen, to the resultant were added water and 2N hydrochloric acid
  5. extractionthe mixture was extracted with ethyl acetate
  6. dry with materialThe organic layer was dried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe obtained residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-4e30d340965041deb32d163a4d305239
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08389511B2

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