HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Nitric Acid → 2,5-Dichloro-4-nitropyridine 1-oxide

HRID 1594102
Notes
Print preview

Reaction equation

HRID 1594102 reaction equation
OS(O)(=O)=O.O=S(=O)=O.[N+:10]([O-:13])(O)=[O:11].[Cl:14][C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][N+:16]=1[O-:22]>OS(O)(=O)=O>[Cl:14][C:15]1[CH:20]=[C:19]([N+:10]([O-:13])=[O:11])[C:18]([Cl:21])=[CH:17][N+:16]=1[O-:22]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 944Nitric AcidHCID 24681Fuming sulfuric acidHCID 113326572,5-Dichloro-pyridine 1-oxide

Product 1

HCID 222840452,5-Dichloro-4-nitropyridine 1-oxide

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent

Procedure

At 0° C., 30% oleum (13 mL) is added slowly to fuming HNO3 (22 mL) and the resulting mixture is added slowly to the solution of 2,5-dichloro-pyridine 1-oxide (5.2 g, 31 mmol) in concentrated H2SO4. After addition, the reaction mixture is warmed to room temperature over 1 hr, then heated to 80° C. for 2 hr. After cooling to room temperature, the mixture is poured into ice (120 g) and precipitate is formed gradually. The solid is collected by filtration and washed with water. The product is obtained as yellow solid. 1H NMR (CDCl3) δ 8.46 (s, 1H), 8.25 (s, 1H).

Workup

  1. additionAfter addition
  2. temperatureheated to 80° C. for 2 hr
  3. temperatureAfter cooling to room temperature
  4. customprecipitate is formed gradually
  5. filtrationThe solid is collected by filtration
  6. washwashed with water
  7. customThe product is obtained as yellow solid

Sources & evidence

ORD record
ord-b9cc95033a43462797c113ebec93a7ce
Source dataset
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07300945B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes