HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841089Generated: October 30, 2026
1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) → HCID 131723176, compound
https://huagongshe.com/reaction/841089
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) | HCID 96831 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 53790515 | HCID 53790515 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 131723176 | HCID 131723176 | — |
Reaction Steps
A solution of N6-benzoyl-2′-O-(trans-2-methoxycyclohexyl)adenosine (0.285 mol) in pyridine (100 mL) is evaporated under reduced pressure to an oil. The residue is redissolved in dry pyridine (300 mL) and 4,4′-dimethoxytriphenylmethyl chloride (DMT-Cl, 10.9 g, 95%, 0.31 mol) added. The mixture is stirred at 25° C. for 16 h and then poured onto a solution of sodium bicarbonate (20 g) in ice water (500 mL). The product is extracted with ethyl acetate (2×150 mL). The organic layer is washed with brine (50 mL), dried over sodium sulfate (powdered) and evaporated under reduced pressure (below 40° C.). The residue is chromatographed on silica gel (400 g, ethyl acetate-hexane 1:1. Selected fractions were combined, concentrated under reduced pressure and dried at 25° C./0.2 mmHg to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06369209B1 |
|---|
| Source dataset | uspto-grants-2002_04 |
|---|
| ORD ID | ord-94ddfb300a7c4ce7bbb77d0a3ec00adb |
|---|
| Source note | uspto-grants-2002_04 |
|---|