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

HRID 1639776
Notes
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Reaction equation

HRID 1639776 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

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

Product 1

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

Reagents, catalysts & solvents 3

HCID 313
Hydrochloric Acid
Solvent
HCID 702EthanolSolvent
HCID 962WaterSolvent

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-1cbf438207524dc98b6243840b6d4f17
Source dataset
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08110585B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes