HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2219800Erstellt: 27. Oktober 2026
Diethyl Ether → Adamantane-1-ylmethyl bromodifluoroacetate
https://huagongshe.com/reaction/2219800
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Tricyclo(3.3.1.1'3,7)dec-1-ylmethanol | HCID 64556 | — |
| Edukt | Bromodifluoroacetyl chloride | HCID 520892 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Adamantane-1-ylmethyl bromodifluoroacetate | HCID 46900814 | 95% |
Reaktionsschritte
A 200 mL, three-necked flask was charged with 4.76 g (31.8 mmol, 1.11 equivalents) of 1-adamantane methanol and 55 g of diethyl ether, followed by stirring to obtain a suspension. Then, 6.15 g (28.6 mmol, 1.0 equivalent) of bromodifluoroacetic chloride were added thereto. The resulting suspension was cooled down to 0° C. by using an iced bath, followed by adding 5.78 g (57.2 mmol, 2.0 equivalents) of triethylamine in a slow dropwise manner. This reaction liquid was allowed to stand with stirring to reach room temperature, followed by stirring at room temperature for 1 hour. Then, 50 g of water were added to wash the reaction liquid. The resulting organic layer was washed with 50 g of saturated sodium hydrogencarbonate, 50 g of saturated brine, and 50 g of water in sequence. Then, it was dried with magnesium sulfate, followed by distilling the solvent off, thereby obtaining 8.78 g of the target adamantane-1-ylmethyl bromodifluoroacetate (yield: 95%, purity: 100%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07414148B2 |
|---|
| Quelldatensatz | uspto-grants-2008_08 |
|---|
| ORD ID | ord-c645125a9b9140bfb9dda74c7b49045e |
|---|
| Quellennotiz | uspto-grants-2008_08 |
|---|