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

Water → HCID 20513415, compound

HRID 1163987
Notes
Print preview

Reaction equation

HRID 1163987 reaction equation
[C-:1]#[N:2].[K+].[I-].[Na+].[CH3:6][O:7][C:8]1[C:13]([CH2:14]Cl)=[CH:12][CH:11]=[CH:10][C:9]=1[O:16][C:17]1[C:18]([CH3:23])=[CH:19][CH:20]=[CH:21][CH:22]=1.O>CS(C)=O>[CH3:6][O:7][C:8]1[C:9]([O:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[CH3:23])=[CH:10][CH:11]=[CH:12][C:13]=1[CH2:14][C:1]#[N:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962WaterHCID 5238Sodium IodideHCID 9032Potassium CyanideHCID 20513505HCID 20513505, compound

Product 1

HCID 20513415HCID 20513415, compoundYield 96.1%

Reagents, catalysts & solvents 1

HCID 679Dimethyl Sulfoxide
Solvent

Procedure

Powdered potassium cyanide (12.50 g) and sodium iodide (28.80 g) were added to a solution of o-tolyl 2-methoxy-3-chloromethylphenyl ether (47.50 g) in dimethylsulfoxide (100 ml) and stirred at room temperature for 30 minutes. The reaction mixture was poured into water and extracted with diethyl ether. The extract was washed with water 3 times, dried over magnesium sulfate and then evaporated to give only 2-[2-methoxy-3-(o-tolyloxy)phenyl]acetonitrile (44.0 g).

Workup

  1. extractionextracted with diethyl ether
  2. washThe extract was washed with water 3 times
  3. dry with materialdried over magnesium sulfate
  4. customevaporated

Sources & evidence

ORD record
ord-91407ad3c63c4cda8e9235513dfca0b7
Source dataset
uspto-grants-1983_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04367238

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes