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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357726Generated: October 27, 2026

Diisopropyl Ether → (R)-2-bromo-1-(3-chlorophenyl)ethanol

https://huagongshe.com/reaction/357726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
ReactantOctanoic anhydrideHCID 69340—
ReactantVinyl laurateHCID 75069—
Reactant2-Bromo-1-(3-chlorophenyl)ethanolHCID 9964694—
Product(R)-2-bromo-1-(3-chlorophenyl)ethanolHCID 11075396—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05841001
Source datasetuspto-grants-1998_11
ORD IDord-2d8910f2b32d45dbbae9fea2b14ba90e
Source noteuspto-grants-1998_11