Acetic Anhydride → 1-{3-Methyl-2-[nitro(phenylsulfanyl)methylidene]imidazolidin-1-yl}ethan-1-one

HRID 1973249Notes

Reaction equation

HRID 1973249 reaction equation
[CH3:1][N:2]1[CH2:6][CH2:5][NH:4][C:3]1=[C:7]([N+:15]([O-:17])=[O:16])[S:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[C:18](OC(=O)C)(=[O:20])[CH3:19]>>[CH3:1][N:2]1[CH2:6][CH2:5][N:4]([C:18](=[O:20])[CH3:19])[C:3]1=[C:7]([N+:15]([O-:17])=[O:16])[S:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1

Participants

3

Reactant 2

HCID 7918Acetic AnhydrideHCID 706390091-Methyl-2-[nitro(phenylsulfanyl)methylidene]imidazolidine

Product 1

HCID 544480941-{3-Methyl-2-[nitro(phenylsulfanyl)methylidene]imidazolidin-1-yl}ethan-1-one

Procedure

20 ml of acetic anhydride and 1.26 g of 1B were heated together at 100° for 1 hour. The resulting mixture was cooled on an ice-bath and filtered to give 1, as a yellow crystals, m.p.: 191°-193° (with decomposition).

Workup

  1. temperatureThe resulting mixture was cooled on an ice-bath
  2. filtrationfiltered
  3. customto give 1

Sources & evidence

ORD record
ord-6e684842b18b46bfb374b92481e88660
Source dataset
uspto-grants-1976_12
Patent number
US03996372

Reaction notes

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