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Hydrochloric Acid → Ethyl 4-amino-5-cyano-2-hydroxy-3-methylbenzoate

HRID 1692502
Notes
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Reaction equation

HRID 1692502 reaction equation
[O-:1][CH2:2][CH3:3].[Na+].[Na].C([O:9][C:10](=O)[CH2:11][CH2:12][CH2:13][CH3:14])(=O)C.C(O[CH:19]=[C:20]([C:23]#[N:24])[C:21]#[N:22])C.Cl.C([OH:28])C>>[CH2:2]([O:1][C:10](=[O:9])[C:11]1[CH:19]=[C:20]([C:21]#[N:22])[C:23]([NH2:24])=[C:13]([CH3:14])[C:12]=1[OH:28])[CH3:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 313Hydrochloric AcidHCID 702EthanolHCID 671522-(Ethoxymethylene)propanedinitrileHCID 2723922Sodium ethoxideHCID 5360545SodiumHCID 21920893Ethylpropionyl acetate

Product 1

HCID 2775029
Ethyl 4-amino-5-cyano-2-hydroxy-3-methylbenzoate
Yield 59%

Procedure

To a solution of sodium ethoxide (1.3 L) (freshly prepared by addition of sodium metal (7.9 g, 0.35 mol) to ethanol (1.3 L)) at 0° C. was added ethylpropionyl acetate (25 g, 0.17 mol) and the solution was stirred at RT for 1 h. To the above solution was added ethoxymethylene malononitrile (21 g, 0.17 mol) at RT and the reaction mixture was refluxed at 80° C. for 2 h. The reaction mixture was cooled, neutralized to pH=7 by addition of 1.5 N HCl and concentrated under vacuum. The obtained residue was diluted with water (100 mL) and filtered. The solid was washed with water and dried under vacuum at 50° C. to give the crude product (27 g). The crude solid was washed with 5% ethyl acetate in pet. ether which gave pure title compound (22.5 g, 59%).

Workup

  1. temperaturethe reaction mixture was refluxed at 80° C. for 2 h
  2. temperatureThe reaction mixture was cooled
  3. concentrationconcentrated under vacuum
  4. additionThe obtained residue was diluted with water (100 mL)
  5. filtrationfiltered
  6. washThe solid was washed with water
  7. customdried under vacuum at 50° C.
  8. customto give the crude product (27 g)
  9. washThe crude solid was washed with 5% ethyl acetate in pet. ether which

Sources & evidence

ORD record
ord-0dce303e64104ca2b6e3d9b983ac9208
Source dataset
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08153800B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes