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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532588Generated: November 1, 2026

Acetic Acid → HCID 10515470, compound

https://huagongshe.com/reaction/1532588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSulfuric AcidHCID 1118—
ReactantHCID 54513693HCID 54513693—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 10515470HCID 1051547058%

Reaction Steps

Methyl 5-deoxy-2,3-di-O-acetyl-L-ribofuranoside (33 g, 15.2 mmol) was dissolved in acetic acid (20 mL) and acetic anhydride (5 mL). The solution was cooled to ice bath temperatures and concentrated sulfuric acid was added dropwise (1 mL). The solution was kept at 5° C. for 4 days, then it was poured into ice water (50 mL) and extracted with 3:1 ethyl acetate hexanes (200 mL and 75 mL). The combined organics were washed with 10% sodium biarbonate (2×50 mL) and water (50 mL). The organic layers were dried, and concentrated and the residue purified on a silica gel column (5×15 cm, 230-400 mesh) with ethyl acetate:hexanes (1:3). Both anomers were observed but were isolated together as a clear oil (2.2 g, 8.8 mmol, 58%); 1H NMR (DMSO-d6) δ5.96 (d, 1H J=1 Hz), 5.23 (d, 1H, H-2, J=5 Hz), 4.96 (t, 1H, H-3, J=5.7 Hz), 4.24-4.16 (m, 1H, H-4), 2.07 (s, 3H, OAc), 2.05 (s, 3H, OAc), 2.02 (s, 3H, OAc), 1.27 (d, 3H, H-5, J=6.3 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204249B1
Source datasetuspto-grants-2001_03
ORD IDord-364fc100af944663ba976f945145d002
Source noteuspto-grants-2001_03