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tert-Butyl mercaptan → Methyl 3-[(tert-butylthio)diazenyl]-6-fluoro-2-methylbenzoate

HRID 1639776
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HRID 1639776 반응식
[NH2:1][C:2]1[C:3]([CH3:13])=[C:4]([C:9]([F:12])=[CH:10][CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].[N:14]([O-])=O.[Na+].C([O-])(=O)C.[K+].[CH3:23][C:24]([SH:27])([CH3:26])[CH3:25]>Cl.O.C(O)C>[C:24]([S:27][N:14]=[N:1][C:2]1[C:3]([CH3:13])=[C:4]([C:9]([F:12])=[CH:10][CH:11]=1)[C:5]([O:7][CH3:8])=[O:6])([CH3:26])([CH3:25])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 6387tert-Butyl mercaptanHCID 517044Potassium AcetateHCID 23668193Sodium NitriteHCID 59334575Benzoic acid, 3-amino-6-fluoro-2-methyl-, methyl ester

생성물 1

HCID 59334531Methyl 3-[(tert-butylthio)diazenyl]-6-fluoro-2-methylbenzoate수율 99.3%

시약·촉매·용매 3

HCID 313
Hydrochloric Acid
용매
HCID 702Ethanol용매
HCID 962Water용매

실험 절차

To a solution of methyl 3-amino-6-fluoro-2-methylbenzoate (12.0 g, 65.5 mmol) in hydrochloric acid (6 N, 200 mL) was added a solution of sodium nitrite (4.97 g, 72.1 mmol) in water (10 mL) at 0° C., and the mixture was stirred for 2 hr. An aqueous potassium acetate solution (30%) was added to the reaction solution at 0° C. to adjust the reaction solution to pH 4, and a solution of 2-methylpropane-2-thiol (8.12 mL, 72.1 mmol) in ethanol (10 mL) was added. The reaction solution was stirred at room temperature for 12 hr, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to give the title compound (18.5 g, yield 99%) as a crudely purified product.

후처리

  1. stirringThe reaction solution was stirred at room temperature for 12 hr
  2. extractionthe mixture was extracted with ethyl acetate
  3. dry with materialThe extract was dried over anhydrous sodium sulfate
  4. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-1cbf438207524dc98b6243840b6d4f17
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08110585B2

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