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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815688Generated: October 27, 2026

Trifluoromethanesulfonic acid → (R)-9-[4-hydroxy-2-(stearoyloxymethyl)butyl]guanine

https://huagongshe.com/reaction/1815688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
Reactant(R)-9-[4,4-diethoxy-2-(stearoyloxymethyl)butyl]guanineHCID 135487833—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(R)-9-[4-hydroxy-2-(stearoyloxymethyl)butyl]guanineHCID 135481053—

Reaction Conditions

Temperature22 °C

Reaction Steps

The product of Example 30, step d) (3.0 kg) was slurried in THF (46 L) at 20° C. A solution of trifluoromethanesulfonic acid (2.25 kg) in 2.25 kg of water (prepared by slowly adding the acid to cold water) was added and the reaction mixture was stirred at 22° C. for 2 hours. The reaction mixture was cooled to 15° C. and quenched with a solution of NaHCO3 (1.5 kg) in water (5.3 kg). Borane t-butylamine complex (powder, 340 g) was added in four portions and then the reaction temperature was increased to 35° C. and stirred for 12 hours. The reaction mixture was added to a solution of 320 g of concentrated HCl (37% aq.) in 115 kg of tap water at 5° C. This mixture was stirred for 30 minutes and the resulting precipitate was filtered and washed with acetonitrile (15 kg). The solids were reprecipitated once or twice from acetone (35 kg). A final precipitation was accomplished by dissolving the product in THF (24 kg) at 65° C., adding water (1.3 kg), cooling to 30° C. and then adding methylene chloride (105 kg). The resulting slurry was cooled to 10° C. and the precipitate was filtered to provide the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878844B2
Source datasetuspto-grants-2005_04
ORD IDord-28ada1b55edf4a4fa0c991c3f30e2458
Source noteuspto-grants-2005_04