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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724854Generated: October 25, 2026

Acetic Acid → 1-(5-O-Acetyl-beta-D-ribofuranosyl)-2,5,6-trichlorobenzimidazole

https://huagongshe.com/reaction/724854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant[(2R,3R,4R,5R)-3,4-diacetoxy-5-(2,5,6-trichlorobenzimidazol-1-yl)tetrahydrofuran-2-yl]methyl acetateHCID 466019—
ReactantPotassium AcetateHCID 517044—
SolventMethanol--water (1/1)HCID 22242641—
Product1-(5-O-Acetyl-beta-D-ribofuranosyl)-2,5,6-trichlorobenzimidazoleHCID 22876557—

Reaction Steps

A mixture of 42 (0.48 g, 1.0 mmol) and KOAc (0.49 g; 5.0 mmol) in MeOH/H2O (20 mL/2 mL) was stirred at room temperature for 24 h. AcOH (0.286 mL, 5.0 mmol) was added and stirring was Continued at room temperature for 15 min. The reaction mixture was evaporated and the residue was partitioned between H2O/CHCl3 (50 mL/50 mL). The CHCl3 layer was washed with sat. NaCl solution (50 mL), dried (Na2SO4), and evaporated. The residue was chromatographed on a silica column (1.9×20 cm, eluted with CHCl3, 1%, 2%, 4% MeOH/CHCl3). Evaporation of fractions 42-51 (15 mL per fraction) and recrystallization from MeOH gave 0.178 g (2 crops, 45%) of 42a as white crystals. MP: 82°-87° C. MS: (El) m/e 393.9875 (20%, M+ =393.9890). 1H NMR (DMSO-d6): d 8.00, 7.96 (2×s, 2, 7-H and 4-H), 5.91 (d, 1, 1-H, J1'-2' =7.5 Hz), 5.59 (d, 1,2'-OH, J2'-2'OH =6.0 Hz), 5.45 (d, 1, 3'-OH, J3'-3'OH =4.5 Hz), 4.44 (dd, 1, 5'-H, J5'-4' =4.5 Hz, J5'-5' =12.5 Hz), 4.42 (m, 1,2'-H, J2'-3' =6.0 Hz), 4.25 (dd, 1,5"-H, J5"-4' =2.5 Hz), 4.17 (m, 1, 4'-H, J3'-4' =3.5 Hz), 4,11 (m, 1, 3'-H), 2.14 (s, 3, 5'-OAc) 13C NMR (DMSO-d6): d 169.95 (COCH3), 142.03 (C2), 140.92 (C3a), 132.30 (C7a), 125.96, 125.86 (C5 and C6), 120.28 (C4), 113.47 (C7), 89.32 (C1'), 82.63 (C4'), 71.41 (C2'), 69.03 (C3'), 63.35 (C5'). 20.56 (COCH3). Anal. Calcd. for C14H13Cl3N2O5 : C, 42.50; H, 3.31; N, 7.08. Found: C, 42.45; H, 3.20; N, 6.97.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705490
Source datasetuspto-grants-1998_01
ORD IDord-1a0c5c3adeb54551917ddac9af0e7551
Source noteuspto-grants-1998_01