Lithium Hydroxide → HCID 58481104, compound
Reaction equation
[C:1]([C:4]1[CH:16]=[CH:15][C:7]([O:8][CH2:9][C:10]([O:12]CC)=[O:11])=[CH:6][C:5]=1[NH2:17])(=[O:3])[CH3:2].[Li+:18].[OH-]>C1COCC1>[C:1]([C:4]1[CH:16]=[CH:15][C:7]([O:8][CH2:9][C:10]([O-:12])=[O:11])=[CH:6][C:5]=1[NH2:17])(=[O:3])[CH3:2].[Li+:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl 2-(4-acetyl-3-aminophenoxy)acetate (TU3205-036) (1.02 g) was dissolved in THF (17 mL) and treated with aqueous LiOH (1 M, 4.3 mL) at ambient temperature for 1 hour. LC-MS analysis showed a clean complete reaction. The reaction mixture was concentrated under reduced pressure, affording lithium 2-(4-acetyl-3-aminophenoxy)acetate (TU3205-042) as a yellowish solid. MS (ESI+): calcd. for free acid 210.10. found 210.10 (MH+).
Workup
- customa clean complete reaction
- concentrationThe reaction mixture was concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-14d33556c0a641fb8d6c5d4fcb5818ef
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08785151B2
Reaction notes
Loading…