HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 905412Erstellt: 24. Oktober 2026
Acetic acid, 2-chloro-, phenylmethyl ester → Tert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrate
https://huagongshe.com/de/reaction/905412
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic acid, 2-chloro-, phenylmethyl ester | HCID 8786 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | tert-butyl 2-hydroxyimino-3-oxobutanoate | HCID 178468384 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Tert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrate | HCID 53811665 | 95,3% |
Reaktionsschritte
To a suspension of tert-butyl 2-hydroxyimino-3-oxobutyrate (56.4 g) and potassium carbonate (62.4 g) in ethyl acetate (300 ml) and N,N-dimethylformamide (60 ml) was added benzyl chloroacetate (60 g), and the mixture was stirred at 40° C. for 7 hours. The reaction mixture was poured into ice-water (1000 ml), and the separated organic layer was washed twice with a saturated aqueous solution of sodium chloride and then dried over magnesium sulfate. Removal of the solvent gave tert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrate (96.3 g) as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04423213 |
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| Quelldatensatz | uspto-grants-1983_12 |
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| ORD ID | ord-c939f19d3f38443cb4ca6640a7d721b6 |
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| Quellennotiz | uspto-grants-1983_12 |
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