HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 247779Erstellt: 25. Oktober 2026
Triethylamine → 1-Monofluoro-2-decyl 4-benzyloxybenzoate
https://huagongshe.com/reaction/247779
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-Benzyloxybenzoylchloride | HCID 3766410 | — |
| Edukt | HCID 14685330 | HCID 14685330 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-Monofluoro-2-decyl 4-benzyloxybenzoate | HCID 54006840 | 38,3% |
Reaktionsschritte
To a solution of 4-benzyloxybenzoic acid chloride (1.3 g) in methylene chloride (25 ml) was slowly added under ice cooling a solution of optically active 1-monofluoro-2-decanol (1.0g, [α]D20 =-7.2) and triethylamine (0.5 g) in methylene chloride (25 ml). The mixture was left to stand until it reached room temperature and stirred for 12 hours. The mixture was poured in ice water and extracted with methylene chloride. The extracted layer was washed with dilute aqueous hydrochloric acid solution, water, 1N aqueous sodium carbonate solution and water, in this order, and dehydrated over anhydrous magnesium sulfate. The solution was distilled under reduced pressure to remove the solvent until a crude product was obtained. The product was subjected to silica-gel column chromatography to obtain 1-monofluoro-2-decyl 4-benzyloxybenzoate (0.78 g). The benzoate and 10% palladium carried on carbon (0.13 g) were added to ethanol and then subjected to de-benzylation under a hydrogen atmosphere to obtain 1-monofluoro-2-decyl-4-hydroxybenzoate (0.6 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05207947 |
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| Quelldatensatz | uspto-grants-1993_05 |
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| ORD ID | ord-86cffd22bc7345b983937e0ed6de99dc |
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| Quellennotiz | uspto-grants-1993_05 |
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