Ammonium → HCID 57753368, compound
Reaction equation
[CH:1]([O:4][C:5]1[CH:13]=[CH:12][C:11]([S:14]([CH3:17])(=[O:16])=[O:15])=[CH:10][C:6]=1[C:7](O)=[O:8])([CH3:3])[CH3:2].[NH4+:18]>>[CH:1]([O:4][C:5]1[CH:13]=[CH:12][C:11]([S:14]([CH3:17])(=[O:16])=[O:15])=[CH:10][C:6]=1[C:7]([NH2:18])=[O:8])([CH3:3])[CH3:2]Participants
3
Procedure
Prepared in analogy to Example A17(a) from 2-Isopropoxy-5-methanesulfonyl-benzoic acid (example B1) and ammonium hydroxyde. MS (m/e): 258.1 ([M+H+, 100%)
Sources & evidence
- ORD record
- ord-53e16b9ae4c94c67926686a5839e7e54
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07557114B2
Reaction notes
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