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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Ribofuranose, 1-acetate 2,3,5-tribenzoate | HCID 10973190 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,3,5-tri-O-benzoyl-alpha-L-ribofuranose | HCID 11048843 | 63.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06512107B2 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-42ab911eb34c41ea9148fd81cda6a91b |
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| Source note | uspto-grants-2003_01 |
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