Hydrochloric Acid → 2-t-Butoxycarbonylmethoxyimino-2-(2-formamidothiazol-4-yl)acetic acid
Reaction equation
C(=O)(O)[O-].[Na+].[CH:6]([NH:8][C:9]1[S:10][CH:11]=[C:12]([C:14](=O)[C:15]([OH:17])=[O:16])[N:13]=1)=[O:7].[O:19]([CH2:21][C:22]([O:24][C:25]([CH3:28])([CH3:27])[CH3:26])=[O:23])[NH2:20].Cl>O>[CH:6]([NH:8][C:9]1[S:10][CH:11]=[C:12]([C:14](=[N:20][O:19][CH2:21][C:22]([O:24][C:25]([CH3:28])([CH3:27])[CH3:26])=[O:23])[C:15]([OH:17])=[O:16])[N:13]=1)=[O:7]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Sodium bicarbonate (4.2 g.) was added to a suspension of 2-(2-formamidothiazol-4-yl)glyoxylic acid (10 g.) in water (500 ml.) to prepare a solution. t-Butyl 2-aminoxyacetate hydrochloric (8.1 g.) was added to the solution and stirred at room temperature for 3 hours while adjusting to pH 6 with sodium bicarbonate. The resultant solution was adjusted to pH 1.5 with hydrochloric acid, salted out and extracted with ethyl acetate three times. The extract was dried over magnesium sulfate and concentrated in vacuo. The residue was pulverized with diethyl ether, and the precipitates were collected by filtration and dried to give 2-(2-formamidothiazol-4-yl)-2-t-butoxycarbonylmethoxyiminoacetic acid (syn isomer, 11.3 g.), mp 117° C. (dec.).
Workup
- customto prepare a solution
- extractionextracted with ethyl acetate three times
- dry with materialThe extract was dried over magnesium sulfate
- concentrationconcentrated in vacuo
- filtrationthe precipitates were collected by filtration
- customdried
Sources & evidence
- ORD record
- ord-eb478159bf534383a7782e8841e278da
- Source dataset
- uspto-grants-1983_02
- Patent number
- US04372952
Reaction notes
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