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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716146Generated: October 31, 2026

Dimethylformamide → Methyl 2-C-methyl-2,3,5-tris-O-(phenylmethyl)-α-D-ribofuranoside

https://huagongshe.com/reaction/716146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 58695680HCID 58695680—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-C-methyl-2,3,5-tris-O-(phenylmethyl)-α-D-ribofuranosideHCID 11810888199.9%

Reaction Steps

1.2 g of sodium hydride was added to an N,N-dimethylformamide solution of 7.2 g of (2S,3R,4R,5R)-4-(benzyloxy)-5-((benzyloxy)methyl)-2-methoxy-3-methyloxolan-3-ol, and thereafter, 5.1 g of benzyl bromide was added dropwise to the mixture at a temperature of 15° C. or lower. The obtained mixture was stirred at room temperature for 1.5 hours. Thereafter, 200 mL of water and 200 mL of ethyl acetate were added to the reaction mixture. The organic layer was fractionated, and it was successively washed with 200 mL of 1 mol/L hydrochloric acid and 200 mL of a saturated sodium chloride aqueous solution. The solvent was distilled away under reduced pressure, so as to obtain 9.0 g of (2S,3R,4R,5R)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)-2-methoxy-3-methyloxolane in the form of a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187514B2
Source datasetuspto-grants-2015_11
ORD IDord-fd154fe8e1ad4aa79107156c94bc30c4
Source noteuspto-grants-2015_11