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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660427Generated: October 30, 2026

Lithium Hydroxide → 6-[(1r,2r)-3-(2-Dimethylaminomethyl-cyclohexyl)-phenoxy]-3,4,5-trihydroxy-tetrahydropyran-2-carboxylic acid

https://huagongshe.com/reaction/660427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantAcetobromo-alpha-D-glucuronic acid methyl esterHCID 88785—
ReactantFaxeladolHCID 9813414—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product6-[(1r,2r)-3-(2-Dimethylaminomethyl-cyclohexyl)-phenoxy]-3,4,5-trihydroxy-tetrahydropyran-2-carboxylic acidHCID 10092925—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 2.33 g (10 mmol) (1R,2R)-3-(2-dimethylaminomethyl-cyclohexyl)-phenol, 3.58 g (9 mmol) acetobromo-α-D-glucuronic acid methyl ester and 0.23 g (9.5 mmol) lithium hydroxide in 23 ml dry methanol was first stirred at 20° C. for 30 minutes, a solution of 0.65 g lithium hydroxide in 25 ml water was then added and the mixture was stirred again for 30 minutes. It was extracted with ethyl acetate and the aqueous phase was adjusted to a pH of 3.5 by addition of acetic acid and extracted again with ethyl acetate. The aqueous phase was evaporated in vacuo and the residue was purified by HPLC. 0.85 g (23% of theory) of the title compound was obtained in this manner in the form of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084497B2
Source datasetuspto-grants-2011_12
ORD IDord-65f8154c8fe84f59983317319f174b5d
Source noteuspto-grants-2011_12