HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462590Generated: October 30, 2026
Isoamyl Nitrite → 2-(Benzhydryloxycarbonylmethoxyimino)-2-(4-thiazolyl)acetic acid
https://huagongshe.com/reaction/462590
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | 2-(2-Aminothiazol-4-yl)-2-(benzhydryloxycarbonylmethoxyimino)acetic acid | HCID 54479990 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Benzhydryloxycarbonylmethoxyimino)-2-(4-thiazolyl)acetic acid | HCID 54436847 | 48% |
Reaction Steps
A solution of isopentyl nitrite (5.9 ml) in tetrahydrofuran (50 ml) was dropwise added to a mixture of 2-(2-aminothiazol-4-yl)-2-(benzhydryloxycarbonyl-methoxyimino)acetic acid (syn isomer) (10.6 g) in tetrahydrofuran (100 ml) at 50° to 55° C. under stirring and the mixture was stirred at 55° to 60° C. for 30 minutes. Tetrahydrofuran was evaporated in vacuo. The residue was dissolved in a mixture of ethyl acetate and water and the mixture was adjusted to pH 7.5 with 20% aqueous solution of potassium carbonate. The separated aqueous layer was adjusted to pH 2.0 with 10% hydrochloric acid and extracted with ethyl acetate. The extract layer was washed with saturated aqueous solution of sodium chloride, dried over magnesium sulfate and evaporated to give 2-(benzhydryloxycarbonylmethoxyimino)-2-(4-thiazolyl)acetic acid (syn isomer) (4.9 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-aad762c7cd65407b88ff939339e6221c |
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| Source note | uspto-grants-1985_05 |
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