Lithium hydroxide, monohydrate → HCID 21460769, compound

HRID 2082516Notes

Reaction equation

HRID 2082516 reaction equation
C(CC[O:12][C:13]([CH2:15][NH:16][C:17]1[C:25]2[C:20](=[CH:21][C:22]([Cl:27])=[CH:23][C:24]=2[Cl:26])[NH:19][C:18]=1[C:28]([O:30]CC)=[O:29])=[O:14])C(C1C=CC=CC=1)=O.[OH2:33].[OH-].[Li+]>O1CCCC1.O>[CH2:18]([N:16]([CH2:15][C:13]([OH:12])=[O:14])[C:17]1[C:25]2[C:20](=[CH:21][C:22]([Cl:27])=[CH:23][C:24]=2[Cl:26])[NH:19][C:18]=1[C:28]([OH:30])=[O:29])[C:17]([C:25]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1)=[O:33]

Participants

5

Procedure

Dissolve 3-[(phenacyl)carbethoxymethyl-amino]-2-carbethoxy-4,6-dichloroindole (0.29 g, 0.626 mmol) in tetrahydrofuran (27 mL) and water (13 mL). Add lithium hydroxide monohydrate (0.158 g, 3.76 mmol) and stir overnight. Pour into 1N hydrchloric acid (100 mL) and extract into ethyl acetate. Dry (MgSO4) and evaporate the solvent in vacuo. Recrystallize (ethyl acetate/hexane) to give the title compound (0.15 g, mp 235°-7° C.

Workup

  1. extractionextract into ethyl acetate
  2. dry with materialDry (MgSO4)
  3. customevaporate the solvent in vacuo
  4. customRecrystallize (ethyl acetate/hexane)

Sources & evidence

ORD record
ord-22bfd5f491c24bbb817fd153d72011e9
Source dataset
uspto-grants-1993_02
Patent number
US05189054

Reaction notes

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