HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1606329Erstellt: 25. Oktober 2026
Acetic Anhydride → 6,8-di-t-butyl-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester
https://huagongshe.com/reaction/1606329
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Triphenylmethyl perchlorate | HCID 10904004 | — |
| Edukt | 6,8-di-t-butyl-2,3-dihydro-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester | HCID 86733276 | — |
| Produkt | 6,8-di-t-butyl-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester | HCID 53843942 | — |
Reaktionsschritte
A mixture of 3.32 parts of 6,8-di-t-butyl-2,3-dihydro-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester, 1.56 parts of triphenylmethyl perchlorate and 30 parts of acetic anhydride was heated at 100°C for thirty minutes. After cooling, the reaction mixture was poured into sodium bicarbonate solution and the resulting mixture was washed with water, dried and the ether was evaporated to give an oil which was chromatographed on silica gel using a 1:1 mixture of chloroform and light petroleum (b.p. 40°-60°C) for elution. This yielded 0.14 parts of 6,8-di-t-butyl-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester, m.p. 130°-131.5°C (after crystallisation from light petroleum (b.p. 40°-60°C). This product was shown by spectral means to be the same as that prepared in Example 13.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US03952104 |
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| Quelldatensatz | uspto-grants-1976_04 |
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| ORD ID | ord-13a592c0f3024c1fa0dc41fa9ebe6241 |
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| Quellennotiz | uspto-grants-1976_04 |
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