HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260333Generated: November 1, 2026
1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) → HCID 13832357, compound
https://huagongshe.com/reaction/2260333
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) | HCID 96831 | — |
| Reactant | HCID 10971862 | HCID 10971862 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13832357 | HCID 13832357 | 75.4% |
Reaction Steps
2'-O-Tosyladenosine (Compound A1) (4.21 g, 10 mmol) and 4,4'-dimethoxytrityl chloride (7.45 g, 22 mmol) were added to anhydrous pyridine (50 ml), and stirred at room temperature for 20 hours. After ice cooling, 50% aqueous pyridine was added, the mixture was extracted with chloroform, and the organic layer was washed successively with aqueous sodium bicarbonate and water, and dried over magnesium sulfate. After distillating away the chloroform, the pyridine was removed by co-evaporation with toluene, and the residue was subjected to silica gel column chromatography eluant: toluene-ethyl acetate-triethylamine→(9:1:0.1) toluene-ethyl acetate-triethylamine-methanol (9:1:0.1:0.2)]. Fractions containing the desired substance were combined and concentrated to give Compound A2 (7.74 g, yield 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05476931 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-0c62cfb2555547829ab054ee8c977a77 |
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| Source note | uspto-grants-1995_12 |
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