HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968369Generated: October 29, 2026
1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) → HCID 23397587, compound
https://huagongshe.com/reaction/968369
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) | HCID 96831 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(9-((2R,4S,5R)-5-((Tert-butyldimethylsilyloxy)methyl)-4-hydroxytetrahydrofuran-2-YL)-9H-purin-6-YL)benzamide | HCID 13833804 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 23397587 | HCID 23397587 | 63.1% |
Reaction Steps
N6-bezoyl-5′-O-(tert-butyldimethylsilyl)-2′-deoxyadenosine (16.1 g) was dissolved in 100 ml of anhydrous pyridine. 4,4′-dimethoxytrityl chloride (12.8 g) and anhydrous pyridine (140 ml) were further added, follow by stirring at 45° C. After the reaction completed, the reaction mixture was neutralized by sodium hydrogen carbonate, and pyridine was distilled off. Extraction using chloroform was carried out and the extract was washed by a saturated aqueous solution of sodium chloride and dried with anhydrous magnesium sulfate. The extract was concentrated and then purified by column chromatography (ethyl acetate/hexane) to obtain 16.7 g of the titled compound (yield: 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06958391B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-375826aa447c49c59a859388bc38af9b |
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| Source note | uspto-grants-2005_10 |
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