Benzyl Alcohol → HCID 11149145, compound

Benzyl alcohol (2.07 mL, 20 mmol) was added to a solution of β-D-ribofuranose-1,2,3,5-tetraacetate (3.18 g, 10 mmol) and zinc bromide (2.25 g, 10 mmol) in toluene (31.8 mL), and the mixture was stirred at ambient temperature for 20 hours. To the resulting solution was added aqueous saturated sodium hydrogen carbonate solution (31.8 mL), for layer separation. To the resulting aqueous layer was added toluene (31.8 mL) for extraction. The resulting two organic layers were combined together, washed with aqueous saturated sodium chloride solution (10 mL), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. To the resulting oily 1-O-benzyl-β-D-ribofuranose-2,3,5-triacetate were added methanol (31.8 mL) and a solution of 28% sodium methoxide in methanol (0.2 mL, 1 mmol), the mixture was stirred at ambient temperature for 2 hours, and the resulting mixture was concentrated under reduced pressure. The resulting oily matter was purified by silica gel column chromatography, to recover the desired 1-O-benzyl-β-D-ribofuranose (2.24 g; yield of 93.2%) as a white solid. Melting point: 95° C.

1. customfor layer separation
2. additionTo the resulting aqueous layer was added toluene (31.8 mL)
3. extractionfor extraction
4. washwashed with aqueous saturated sodium chloride solution (10 mL)
5. dry with materialdried over anhydrous magnesium sulfate
6. concentrationconcentrated under reduced pressure
7. additionTo the resulting oily 1-O-benzyl-β-D-ribofuranose-2,3,5-triacetate were added methanol (31.8 mL)
8. concentrationthe resulting mixture was concentrated under reduced pressure
9. customThe resulting oily matter was purified by silica gel column chromatography

ORD record

ord-48a73defabb2454cb87aadb8b83d523b

Source dataset

uspto-grants-2004_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06800742B2