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

Water → 1-methyl-3-formyl-4-hydroxy-2(1H)-quinolinone

HRID 1586070
Notes
Print preview

Reaction equation

HRID 1586070 reaction equation
[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5](=[O:12])[C:4](=[CH:13]N(C)C)[C:3]1=[O:17].[OH2:18]>>[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([OH:12])=[C:4]([CH:13]=[O:18])[C:3]1=[O:17]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 962WaterHCID 536541001-methyl-3-dimethylaminomethylene-(1H)-quinolin-2,4-dione

Product 1

HCID 1354542351-methyl-3-formyl-4-hydroxy-2(1H)-quinolinone

Procedure

The product from Step (1) was dissolved in distilled water (50 ml) by gentle warming and then the resulting solution was filtered. The clear filtrate was cooled in an ice bath and acidified to pH3 with mineral acid. The resulting crystalline precipitate was washed with water and dried to give 1-methyl-3-formyl-4-hydroxy-2(1H)-quinolinone. That the expected product was obtained was confirmed by the spectral data: MS: m/e 203 (M.+); NMR (CDCl3): δ3.6 (s, 3H, NCH3), 10.28 (s, 1H, CHO) ppm.

Workup

  1. temperatureby gentle warming
  2. filtrationthe resulting solution was filtered
  3. temperatureThe clear filtrate was cooled in an ice bath
  4. wash
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
The resulting crystalline precipitate was washed with water
  • customdried
  • Sources & evidence

    ORD record
    ord-cdb661e20c6346808c48d55969ad120c
    Source dataset
    uspto-grants-1999_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05942522

    Reaction notes

    Loading…