HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589621Generated: October 30, 2026
HCID 88615492, compound → HCID 10870340, compound
https://huagongshe.com/reaction/1589621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 88615492 | HCID 88615492 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10870340 | HCID 10870340 | 80.3% |
Reaction Steps
In 1.2 l of tetrahydrofuran is dissolved 20 g (45.9 mmol) of p-nitrobenzyl (Z)-2-(2-amino-4-thiazolyl)-2-(t-butoxycarbonylmethoxyimino)acetate and, after addition of 20 g of 10% palladium-on-carbon, hydrogen gas is bubbled into the solution. After completion of the reaction, the catalyst is filtered off, and the filtrate is poured into 300 ml of water. The mixture is adjusted to about pH 8 with 5% aqueous sodium bicarbonate and washed with three 200-ml portions of ethyl acetate. The aqueous layer is adjusted to pH about 2 with 10% HCl and cooled to 5° C. or lower. The resulting crystalline precipitate is collected by filtration, washed with water and dried under reduced pressure to give 11.1 g of (Z)-2-(2-amino-4-thiazolyl)-2-(t-butoxycarbonylmethoxyimino)acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04572801 |
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| Source dataset | uspto-grants-1986_02 |
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| ORD ID | ord-8c09f5f0c3c54f87b1845bc857726414 |
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| Source note | uspto-grants-1986_02 |
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