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

Ethanol → HCID 66765121, compound

HRID 1466962
Notes
Print preview

Reaction equation

HRID 1466962 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:12]([F:15])([F:14])[F:13])=[C:6]([CH2:8][C:9]([OH:11])=[O:10])[CH:7]=1.OS(O)(=O)=O.[CH3:21][CH2:22]O>>[CH2:21]([O:10][C:9](=[O:11])[CH2:8][C:6]1[CH:7]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=1[C:12]([F:13])([F:14])[F:15])[CH3:22]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 27781225-Chloro-2-(trifluoromethyl)phenylacetic acid

Product 1

HCID 66765121HCID 66765121, compound

Procedure

To a stirred solution of (5-Chloro-2-trifluoromethyl-phenyl)-acetic acid (10.0 g, 47.2 mmol) in absolute EtOH (300 mL) at room temperature was added concentrated H2SO4 (4 mL) and the mixture was warmed to reflux. After 4 hrs, the reaction was cooled to room temperature, evaporated under reduced pressure, diluted with DCM (500 mL) and stirred over solid K2CO3. After 1 hr, the resulting mixture was filtered and concentrated to dryness to afford the title compound.

Workup

  1. temperature
the mixture was warmed to reflux
  • customevaporated under reduced pressure
  • additiondiluted with DCM (500 mL)
  • waitAfter 1 hr
  • filtrationthe resulting mixture was filtered
  • concentrationconcentrated to dryness
  • Sources & evidence

    ORD record
    ord-56bda05d78604df3bb1491a20877192c
    Source dataset
    uspto-grants-2015_04
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US09000025B2

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes