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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716145Generated: October 30, 2026

Ammonium Chloride → HCID 58695680, compound

https://huagongshe.com/reaction/716145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 3,5-di-O-benzyl-alpha-D-erythro-pentofuranosid-2-uloseHCID 53493674—
ReactantHCID 178420675HCID 178420675—
ReactantHCID 178467822HCID 178467822—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 58695680HCID 58695680—

Reaction Conditions

Temperature0 °C

Reaction Steps

92 mL of a 1 mol/L methyl magnesium bromide/tetrahydrofuran solution and 23 mL of a 3 mol/L methyl magnesium bromide/diethyl ether solution were added dropwise to a solution of 23.2 g of (2S,4R,5R)-4-(benzyloxy)-5-((benzyloxy)methyl)-2-methoxyoxolane-3-one in 100 mL of tetrahydrofuran at −40° C., and the obtained mixture was then stirred at the same temperature as described above for 30 minutes. Thereafter, the temperature of the reaction mixture was increased to 0° C. over 1 hour, and 500 mL of a saturated ammonium chloride aqueous solution and 500 mL of ethyl acetate were then added to the mixture. The organic layer was fractionated, and it was washed with 300 mL of a saturated sodium chloride aqueous solution and was then dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure, and the obtained residue was then purified by silica gel column chromatography, so as to obtain 12.0 g of (2S,3R,4R,5R)-4-(benzyloxy)-5-((benzyloxy)methyl)-2-methoxy-3-methyloxolan-3-ol 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-650ece3391554f1fb52a80fd8367f578
Source noteuspto-grants-2015_11