Benzamide, 2-(aminosulfonyl)-N,N-diethyl-4-methoxy-6-(1-methylethyl)- → 4-Isopropyl-6-methoxysaccharin

HRID 129039

Reaction equation

HRID 129039 reaction equation
N[S:2]([C:5]1[CH:17]=[C:16]([O:18][CH3:19])[CH:15]=[C:14]([CH:20]([CH3:22])[CH3:21])[C:6]=1[C:7]([N:9](CC)CC)=[O:8])(=[O:4])=[O:3]>C(O)(=O)C>[CH:20]([C:14]1[CH:15]=[C:16]([O:18][CH3:19])[CH:17]=[C:5]2[C:6]=1[C:7](=[O:8])[NH:9][S:2]2(=[O:4])=[O:3])([CH3:22])[CH3:21]

Participants

3

Reactant 1

HCID 10336632Benzamide, 2-(aminosulfonyl)-N,N-diethyl-4-methoxy-6-(1-methylethyl)-

Product 1

HCID 101473624-Isopropyl-6-methoxysaccharinYield 91%

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

A solution of 2.aminosulfonyl-6-isopropyl-4-methoxy-N,N-diethylbenzamide (429.6 g) in acetic acid (1.5 L) was refluxed for 20 hours, then cooled to room temperature. The solvent was removed under vacuum. The oily residue was dissolved in water (6 L) and the pH was adjusted to 1 with hydrochloric acid (6N). The crude product was collected by filtration, washed with water (2 L), dried at 60° C. under vacuum for 18 hours and recrystallized from ethyl acetate-hexane to give 4-isopropyl-6-methoxysaccharin (303 g, 91% yield, m.p. 188° C.).

Workup

  1. customThe solvent was removed under vacuum
  2. dissolutionThe oily residue was dissolved in water (6 L)
  3. filtrationThe crude product was collected by filtration
  4. washwashed with water (2 L)
  5. customdried at 60° C. under vacuum for 18 hours
  6. customrecrystallized from ethyl acetate-hexane

Sources & evidence

ORD record
ord-0a8197a401934a08a1fab500f722f634
Source dataset
uspto-grants-1995_11
Patent number
US05466701

Linked notes

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