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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160477Generated: October 30, 2026

Sulfuric Acid → 5-Chloro-2-[((2S)-2-fluoro-3-hydroxypropyl)oxy]benzonitrile

https://huagongshe.com/reaction/1160477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant2-Methylbenzyl alcoholHCID 6994—
ReactantSodium HydroxideHCID 14798—
Reactant5-Chloro-2-[[(2R)-2-fluoro-3-(trityloxy)propyl]oxy]benzonitrileHCID 68419996—
Product5-Chloro-2-[((2S)-2-fluoro-3-hydroxypropyl)oxy]benzonitrileHCID 5951642588%

Reaction Conditions

Temperature60 °C

Reaction Steps

5-Chloro-2-[[(2R)-2-fluoro-3-(trityloxy)propyl]oxy]benzonitrile (460 g, 0.97 mol) was suspended in a toluene-methanol mixture (4.8 L/3.22 L) at room temperature and then concentrated sulfuric acid (3.1 mL, 0.06 mol) was added to the reaction mixture, followed by stirring the reaction mixture at the same temperature for 18.5 hours. A 1N sodium hydroxide aqueous solution was added to the reaction mixture at room temperature to adjust the pH to 14 or more, followed by subjecting the reaction mixture to vacuum concentration. Ethyl acetate (2.1 L) and water (1.2 L) were added to the residue to separate an organic layer, followed by washing the organic layer twice with water (1.2 L) before vacuum concentration. Ethyl acetate (0.7 L) was added to the resultant crude crystal, which was then heated to 60° C. for complete dissolution. Heptane (3.8 L) was then added to the reaction mixture, followed by cooling and the filtration of the precipitated crystal to obtain 196 g of the title compound (yield: 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816405B2
Source datasetuspto-grants-2010_10
ORD IDord-99d0848b76d2419285b2f6c405cd6aea
Source noteuspto-grants-2010_10