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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766650Generated: October 31, 2026

Thionyl Chloride → 4-(4-Benzyloxy-3-chloromethylphenoxy)-5-methyl-7-nitroindane

https://huagongshe.com/reaction/1766650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant[2-Benzyloxy-5-(5-methyl-7-nitroindan-4-yloxy)phenyl]methanolHCID 23031098—
SolventDiethyl EtherHCID 3283—
Product4-(4-Benzyloxy-3-chloromethylphenoxy)-5-methyl-7-nitroindaneHCID 23031167—

Reaction Steps

[2-benzyloxy-5-(5-methyl-7-nitroindan-4-yloxy)phenyl]methanol (2.48 g) was dissolved in diethyl ether. After adding dropwise thionyl chloride (5 mL) under ice-cooling with stirring, the mixture was stirred at room temperature for 6 hours. The reaction mixture was evaporated under reduced pressure to dryness. After adding water (10 mL), the residue was extracted with diethyl ether. The organic layer was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to give the title compound (2.04 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230031B2
Source datasetuspto-grants-2007_06
ORD IDord-0580df68c11b4842a5f286b946988595
Source noteuspto-grants-2007_06