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

Hydrochloric Acid → 6-Benzoxazoleacetic acid, 2-phenyl-, ethyl ester

HRID 2397238
Notes
Print preview

Reaction equation

HRID 2397238 reaction equation
[C:1]1([C:7]2[O:8][C:9]3[CH:15]=[C:14]([CH2:16][C:17]([OH:19])=[O:18])[CH:13]=[CH:12][C:10]=3[N:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[CH2:21](O)[CH3:22]>>[CH2:21]([O:18][C:17](=[O:19])[CH2:16][C:14]1[CH:13]=[CH:12][C:10]2[N:11]=[C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[O:8][C:9]=2[CH:15]=1)[CH3:22]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 439316-Benzoxazoleacetic acid, 2-phenyl-

Product 1

HCID 399486-Benzoxazoleacetic acid, 2-phenyl-, ethyl ester

Procedure

A solution of 2-phenyl-6-benzoxazolylacetic acid (20 gm) in ethanol (200 ml) was heated under reflux for 6 hr., during which time dry hydrogen chloride gas was passed through the solution. The residual oil on evaporation of the solution was extracted with ether and this solution was evaporated to dryness. The solid formed was recrystallised from toluene/petroleum ether to yield while crystals of ethyl-2-phenyl-6-benzoxazolylacetate, m.p. 76° C.

Workup

  1. temperature
under reflux for 6 hr
  • customThe residual oil on evaporation of the solution
  • extractionwas extracted with ether
  • customthis solution was evaporated to dryness
  • customThe solid formed
  • customwas recrystallised from toluene/petroleum ether
  • Sources & evidence

    ORD record
    ord-98f674bd2bb7490489356d1c90340235
    Source dataset
    uspto-grants-1977_05
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04021440

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes