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Water → 2,4-Dibromo-6-(difluoromethanesulfonyl)aniline

HRID 1995458
Notes
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Reaction equation

HRID 1995458 reaction equation
[NH2:1][C:2]1[C:7]([Br:8])=[CH:6][C:5]([Br:9])=[CH:4][C:3]=1[S:10]([OH:12])=[O:11].O.Cl[CH:15]([F:17])[F:16]>C(O)(C)C.[OH-].[Na+]>[Br:8][C:7]1[CH:6]=[C:5]([Br:9])[CH:4]=[C:3]([S:10]([CH:15]([F:17])[F:16])(=[O:12])=[O:11])[C:2]=1[NH2:1]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 962Water2×HCID 6372ChlorodifluoromethaneHCID 13218906HCID 13218906, compound

Product 1

HCID 132189132,4-Dibromo-6-(difluoromethanesulfonyl)aniline

Reagents, catalysts & solvents 2

HCID 3776IsopropanolSolventHCID 14798Sodium Hydroxide
Solvent

Conditions

Temperature
40 °C

Procedure

A solution of 2-amino-3,5-dibromobenzenesulfinic acid (7.98 g; 0.025 mol) in a mixture of isopropyl alcohol (100 ml) and sodium hydroxide (8.0 g of 50% aqueous) and water (2 ml) is warmed to 40° C. Chlorodifluoromethane is added slowly through a gas inlet tube over a period of 3 hours. The reaction mixture exotherms to 55° C. The reaction mixture is poured into water (500 ml) and the solution is extracted with methylene chloride (2×100 ml). The combined extracts are washed with saturated NaHCO3 (100 ml), saturated NaCl (100 ml), then dried over MgSO4. The solvent is evaporated under vacuum yield 0.9 g of the title product, m.p. 84°-88° C.

Workup

  1. customexotherms to 55° C
  2. extractionthe solution is extracted with methylene chloride (2×100 ml)
  3. washThe combined extracts are washed with saturated NaHCO3 (100 ml), saturated NaCl (100 ml)
  4. dry with materialdried over MgSO4
  5. customThe solvent is evaporated under vacuum yield 0.9 g of the title product, m.p. 84°-88° C.

Sources & evidence

ORD record
ord-184d3148618a41c094bdef81d50d731c
Source dataset
uspto-grants-1983_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04404402

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes