HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1267622Erstellt: 26. Oktober 2026
Hydrochloric Acid → 3',4',5'-Trimethoxycinnamyl alcohol
https://huagongshe.com/reaction/1267622
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 3-(3,4,5-Trimethoxyphenyl)acrylic acid | HCID 7021 | — |
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 3',4',5'-Trimethoxycinnamyl alcohol | HCID 73924 | — |
Reaktionsschritte
3,4,5-Trimethoxycinnamic acid (1.5 g) was dissolved in THF (100 mL), triethylamine (0.64 mL) was added to the solution under ice cooling, and ethyl chlorocarbonate (0.44 mL) was then added dropwise thereto. After stirring the resultant mixture at room temperature for 1 hour, sodium borohydride (477 mg) was added to the mixture under ice cooling. After stirring the resultant mixture at room temperature for 1 hour, diluted hydrochloric acid was added to the reaction mixture to conduct extraction with chloroform. The resultant organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1) to obtain the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06552188B2 |
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| Quelldatensatz | uspto-grants-2003_04 |
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| ORD ID | ord-b1259147d3e147f487dc04a96e5576dc |
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| Quellennotiz | uspto-grants-2003_04 |
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