2-Methyl-2-butene → HCID 22380897, compound

HRID 895714

Reaction equation

HRID 895714 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([O:13][C:14]1[CH:19]=[CH:18][C:17]([N+:20]([O-:22])=[O:21])=[CH:16][C:15]=1[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=1[CH:29]=[O:30])[CH:7]=[CH:6]2)#[N:2].CC(=CC)C.O.O.P([O-])(O)(O)=[O:39].[Na+].Cl([O-])(=O)=O.[Na+].O.Cl>C(#N)C.O>[N+:20]([C:17]1[CH:18]=[CH:19][C:14]([O:13][C:8]2[CH:7]=[CH:6][C:5]3[C:10](=[CH:11][CH:12]=[C:3]([C:1]#[N:2])[CH:4]=3)[CH:9]=2)=[C:15]([C:23]2[C:24]([C:29]([OH:39])=[O:30])=[CH:25][CH:26]=[CH:27][CH:28]=2)[CH:16]=1)([O-:22])=[O:21]

Participants

7

Reactant 5

HCID 105532-Methyl-2-buteneHCID 516902Sodium ChlorateHCID 21885828Hydrate;hydrochlorideHCID 22380967HCID 22380967, compoundHCID 23673460Sodium Phosphate, Monobasic, Dihydrate

Product 1

HCID 22380897HCID 22380897, compound

Reagents, catalysts & solvents 1

HCID 18373917Acetonitrile--water (1/1)Solvent

Procedure

The compound (4-(6-cyano-2-naphthyloxy)-3-(2-formylphenyl)nitrobenzene) (800 mg) obtained in a previous production example, 2-methyl-2-butene (1.4 ml) and sodium dihydrogen phosphate dihydrate (2 g) were dissolved in acetonitrile:water (2:1, 50 ml) and then sodium chlorate (1 g) was added. After reaction for one hour at room temperature, 1 N hydrochloric acid water was added and extraction was performed with ethyl acetate. The ethyl acetate layer was washed with 1N hydrochloric acid water and saturated saline and then dried over magnesium sulfate, and the solvent was distilled off to obtain 5′-nitro-2′-(6-cyano-2-naphthyloxy)-1,1′-biphenyl-2-carboxylic acid (800 mg). This was dissolved in toluene without purification and subjected to the same process as in Production Example 1 to obtain t-butyl 2′-(6-cyano-2-naphthyloxy)-5′-nitro-1,1′-biphenyl-2-carboxylate.

Workup

  1. customAfter reaction for one hour at room temperature
  2. extractionextraction
  3. washThe ethyl acetate layer was washed with 1N hydrochloric acid water and saturated saline
  4. dry with materialdried over magnesium sulfate
  5. distillationthe solvent was distilled off

Sources & evidence

ORD record
ord-cd966038481b468884d58abc9f497da2
Source dataset
uspto-grants-2005_07
Patent number
US06916837B2

Linked notes

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