HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612835Generated: October 30, 2026
1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) → Cytidine
https://huagongshe.com/reaction/612835
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) | HCID 96831 | — |
| Reactant | N-Benzoyl-2'-O-methylcytidine | HCID 13852838 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Cytidine | HCID 6175 | — |
Reaction Steps
N4 -Benzoyl-2'-O-methylcytidine (28 g, 0.077 mol) was evaporated under reduced pressure to an oil with pyridine (400 mL). To the residue was added 4,4'-dimethoxytriphenylmethyl chloride (DMT-Cl, 28.8 g, 0.085 mol) and pyridine (400 mL). The mixture was stirred at 25° C. for 2 h and then quenched by the addition of methanol (10 mL) for 30 min. The mixture was concentrated under reduced pressure and the residue was chromatographed on silica gel (500 g, hexanes-ethyl acetatetriethylamine 60:40:1 and then ethyl acetate-triethylamine 99:1). The appropriate fractions were combined, evaporated under reduced pressure and dried at 40° C./0.2 mmHg for 2 h to give 26 g (74%, 16% from cytidine) of foam; TLC homogenous (Rf 0.45, ethyl acetate); PMR (DMSO) δ 11.3 (H-N4), 8.4-6.9 (H-6, H-5, Bz), 5.95 (H-1'), 5.2 (HO-3'), 3.7 (s, 6, CH3O-trit.), 3.5 (s, 3, CH3O-2')
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06005087 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-604b19ce44944bad9f718cfb95439862 |
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| Source note | uspto-grants-1999_12 |
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