HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 357726Erstellt: 25. Oktober 2026
Diisopropyl Ether → (R)-2-bromo-1-(3-chlorophenyl)ethanol
https://huagongshe.com/reaction/357726
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropyl Ether | HCID 7914 | — |
| Edukt | Octanoic anhydride | HCID 69340 | — |
| Edukt | Vinyl laurate | HCID 75069 | — |
| Edukt | 2-Bromo-1-(3-chlorophenyl)ethanol | HCID 9964694 | — |
| Produkt | (R)-2-bromo-1-(3-chlorophenyl)ethanol | HCID 11075396 | — |
Reaktionsschritte
To a mixture of 100 mg (0.4 mmol) of 2-bromo-1-(3-chlorophenyl)ethanol, 10 mg of TOYOCHIMU LIP (available from Toyobo Co., Ltd.) and 100 mg (0.31 mmol) of n-caprylic anhydride or 61 mg (0.27 mmol) of vinyl laurate as an acylating agent was added isopropyl ether to make the total volume 1 ml. The reaction mixtures were respectively allowed to undergo reaction at a temperature of 27° C. for 30 hours. After the termination of the reaction, the reaction system was subjected to centrifugal filtration to remove the supernatant. To the reaction system was then added another batch of 2-bromo-1-(3-chlorophenyl)ethanol, the acylating agent and diisopropyl ether to make the total volume 1 ml. The same reaction was then repeated twice. The initial rate and total activity at the various steps are set forth in Table 5. The initial rate is represented relative to that at the 1st step as 100%. Activity=total amount of converted BH/enzyme weight.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05841001 |
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| Quelldatensatz | uspto-grants-1998_11 |
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| ORD ID | ord-2d8910f2b32d45dbbae9fea2b14ba90e |
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| Quellennotiz | uspto-grants-1998_11 |
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