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Isopropyl iodide → 6-nitro-3-isopropyl-2(3H)-benzothiazolone

HRID 896124
Notes
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Reaction equation

HRID 896124 reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][C:7]2[NH:8][C:9](=[O:11])[S:10][C:6]=2[CH:5]=1)([O-:3])=[O:2].N12CCCN=C1CC[CH2:17][CH2:16][CH2:15]2.IC(C)C>CN(C)C=O.O>[N+:1]([C:4]1[CH:13]=[CH:12][C:7]2[N:8]([CH:16]([CH3:17])[CH3:15])[C:9](=[O:11])[S:10][C:6]=2[CH:5]=1)([O-:3])=[O:2]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 6362Isopropyl iodideHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 6415712(3H)-Benzothiazolone, 6-nitro-

Product 1

HCID 218780606-nitro-3-isopropyl-2(3H)-benzothiazolone

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228
Dimethylformamide
Solvent

Conditions

Temperature
50 °C

Procedure

A stirred solution of 6-nitro-2-benzothiazolinone (5.0 g, 25.5 mmol) in anhydrous N,N-dimethylformamide (51 mL) under N2 is treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (4.96 mL, 33.1 mmol) dropwise. Following a slight exotherm, the reaction mixture is heated up to 50° C. and treated with 2-iodopropane (12.7 mL, 127 mmol). The resulting mixture is quickly heated up to 75° C., stirred at this temperature for 40 mins, cooled to ambient temperature and diluted with ice (100 mL) and water (100 mL). The precipitate is isolated by filtration and recrystallized from ethyl acetate/hexanes to give the title compound, mp 138-142° C.

Workup

  1. temperatureThe resulting mixture is quickly heated up to 75° C.
  2. temperaturecooled to ambient temperature
  3. customThe precipitate is isolated by filtration
  4. customrecrystallized from ethyl acetate/hexanes

Sources & evidence

ORD record
ord-60dfaa3b7716471bb5b52ba7501987ed
Source dataset
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06919329B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes