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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337365Generated: October 26, 2026

Water → 4-Methoxy-5-methyl-2-nitrophenyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/337365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant4-Methoxy-5-methyl-2-nitrophenolHCID 57418664—
SolventDichloromethaneHCID 6344—
Product4-Methoxy-5-methyl-2-nitrophenyl 4-methylbenzenesulfonateHCID 8670326881.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-methoxy-5-methyl-2-nitro phenol (8.0 g) in methylene chloride (80 mL) was added p-toluenesulfonyl chloride (9.15 g) at room temperature under nitrogen atmosphere. The mixture was cooled to 0° C. To this mixture triethylamine (4.86 g) was added and stirred for 2 h. Then the reaction mixture was poured into water (150 mL) and extracted with methylene chloride (150 mL). The organic layer was washed with water (100 mL) and saturated brine (50 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography over silica gel using hexane/ethyl acetate (9:1) to give the title compound (12.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889727B2
Source datasetuspto-grants-2014_11
ORD IDord-4e7cff8f2e564713a42a9ab76bfbd568
Source noteuspto-grants-2014_11