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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727318Generated: November 2, 2026

Anisole → HCID 68851738, compound

https://huagongshe.com/reaction/1727318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 66739673HCID 66739673—
SolventMethanolHCID 887—
ProductHCID 68851738HCID 68851738—

Reaction Steps

In a 50 mL flask with 9-[cis-4-(benzyloxymethyl)-cyclobutyl]adenine (63.2 mg, 0.2 mmol) inside, dry anisole 5 mL was added to give a light yellow solution under argon. In another 10 mL flask with AlCl3 inside, dry anisole 2 mL was added under argon to give a totally clear red solution. This solution was added drop by drop to the first flask to give a red solution. After stirring at ambient temperature for 1 hr, TLC showed no starting material. The reaction mixture was cooled to 0° C. and dry MeOH was added drop by drop until the red color disappeared. The solvents were removed by rotovap to give an off-white solid and this was purified by silica gel flash chromatography (CH2Cl2:MeOH=15:1) to yield a white solid (33 mg, 72.4%, Rf=0.15 (CH2Cl2:MeOH=15:1)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495006B2
Source datasetuspto-grants-2009_02
ORD IDord-f27ce29aec7840d094bf8fb2a129305f
Source noteuspto-grants-2009_02