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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636043Generated: October 27, 2026

Hydrochloric Acid → 1,3,5-tri-O-benzoyl-alpha-L-ribofuranose

https://huagongshe.com/reaction/1636043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantRibofuranose, 1-acetate 2,3,5-tribenzoateHCID 10973190—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1,3,5-tri-O-benzoyl-alpha-L-ribofuranoseHCID 1104884363.7%

Reaction Steps

HCl (gas) was bubbled for 1.5 hours into a solution of 50 g (99.16 mole) of the compound (12) dissolved in 460 ml of anhydrous dichloromethane and 7.5 ml of acetyl chloride at 0° C. The resulting solution was kept in a refrigerator for 12 hours and then evaporated in vacuo. The residue was coevaporated with toluene (3×150 ml) at 45° C. and redissolved in 105 ml of acetonitrile. To this solution, 13 ml of water was added dropwise at 0° C. A white solid began to precipitate from the mixture after 30 minutes, after which the mixture was kept in a refrigerator for 2 hours to induce additional precipitation. After filtration of the resulting solid, the filter cake was. carefully washed with cold diethylether to remove the reaction by-product 1-hydroxy-isomer, which is indistinguishable by TLC from the compound (13). The white solid thereby obtained was dissolved in ethyl acetate. The solution was washed with saturated sodium bicarbonate to remove the remaining HCl, dried over MgSO4 and filtered. The solvent was removed from the filtrate to obtain 29.2 g (Yield: 63.7%) of the compound (13) in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06512107B2
Source datasetuspto-grants-2003_01
ORD IDord-42ab911eb34c41ea9148fd81cda6a91b
Source noteuspto-grants-2003_01