HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462594Generated: October 30, 2026
Water → Benzhydryl 2-t-butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetate
https://huagongshe.com/reaction/462594
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | Benzhydryl 2-t-butoxycarbonylmethoxyimino-2-(2-aminothiazol-4-yl)acetate | HCID 53827226 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzhydryl 2-t-butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetate | HCID 54223791 | 45.5% |
Reaction Steps
A solution of t-butyl nitrite (1.7 g) in tetrahydrofuran (10 ml) was dropwise added to a solution of benzhydryl 2-t-butoxycarbonylmethoxyimino-2-(2-aminothiazol-4-yl)acetate (syn isomer) (5 g) in tetrahydrofuran (50 ml) at 50° to 53° C. under stirring and the mixture was stirred at the same temperature at 25 minutes. The reaction mixture was poured into a mixture of ethyl acetate and water and the organic layer was separated. The organic layer was washed with brine and dried over magnesium sulfate. The solution was evaporated and the residue was subjected to column chlomatography on silica gel. The elution was carried out with a mixture of benzene and ethyl acetate (19:1) and the eluates containing the object compound were evaporated to give benzhydryl 2-t-butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetate (syn isomer) (2.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04515788 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-e221332a3a5444e3aac1a75f1113c757 |
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| Source note | uspto-grants-1985_05 |
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