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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 53790515HCID 53790515—
SolventPyridineHCID 1049—
ProductHCID 131723176HCID 131723176—

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369209B1
Source datasetuspto-grants-2002_04
ORD IDord-94ddfb300a7c4ce7bbb77d0a3ec00adb
Source noteuspto-grants-2002_04