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Hydrochloric Acid → HCID 888434, compound

HRID 846211
Notes
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Reaction equation

HRID 846211 reaction equation
[CH3:1][C:2]([C:5]1[CH:26]=[CH:25][C:8]([C:9]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([O:18][CH2:19][C:20]([O:22]CC)=[O:21])=[CH:14][CH:13]=2)=[O:10])=[CH:7][CH:6]=1)([CH3:4])[CH3:3].[OH-].[Na+].Cl>>[CH3:4][C:2]([C:5]1[CH:26]=[CH:25][C:8]([C:9]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([O:18][CH2:19][C:20]([OH:22])=[O:21])=[CH:14][CH:13]=2)=[O:10])=[CH:7][CH:6]=1)([CH3:1])[CH3:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 14698592HCID 14698592, compound

Product 1

HCID 888434HCID 888434, compound

Procedure

2.0 g. 4-(1,1-Dimethylethyl)-N-[4-(ethoxycarbonylmethoxy)-phenyl]-benzamide (Example 31) are heated in 20 ml. 2N aqueous sodium hydroxide solution, then acidified with concentrated hydrochloric acid, filtered off with suction and washed with water. After recrystallisation from ethyl acetate, there is obtained 1.2 g. (65% of theory) of the title compound; m.p. 179°-181° C.

Workup

  1. filtrationfiltered off with suction
  2. washwashed with water
  • customAfter recrystallisation from ethyl acetate
  • customthere is obtained 1.2 g
  • Sources & evidence

    ORD record
    ord-7a544cf21af2493fbe2aa877bb2b26c5
    Source dataset
    uspto-grants-1992_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05135949

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes