Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647372Generated: October 30, 2026

Dimethyl Sulfate → 2-Methoxy-5-methyl-1-(trifluoromethyl)naphthalene

https://huagongshe.com/reaction/647372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Methyl-1-(trifluoromethyl)naphthalen-2-olHCID 15568760—
SolventDimethylformamideHCID 6228—
Product2-Methoxy-5-methyl-1-(trifluoromethyl)naphthaleneHCID 1556876190%

Reaction Conditions

Temperature25 °C

Reaction Steps

Dimethylsulfate (1.13 g, 8.75 mmol, 0.85 mL) was added to a stirred suspension of 5-methyl-1-(trifluoromethyl)-2-naphthalenol (1.8 g, 7.96 mmol) and potassium carbonate (2.2 g, 15.9 mmol) in dimethylformamide (20 mL). After stirring the reaction mixture for 2 hr at 25° C., the solid in the reaction mixture was removed by filtration. The filtrate was extracted with hexane (400 mL). The extract was washed with brine, dried (MgSO4) and concentrated to dryness giving 1.7 g (90% yield) of the title compound. This product was used for the reaction described in the next example. A sample of the product, recrystallized from hexane, had mp 70°-71° C.; nmr (CDCl3) δ 2.65 (s, 3H), 3.95 (s, 3H), 7.2 (m, 2H), 7.35 (q, J=8 Hz, 1H), 8.0 (m, 1H), 8.1 (d, J=9 Hz, 1H); ir (CHCl3) 1390, 1340, 1280, 1255, 1245, 1110, 1095, 1085,1045 cm-1 ; uvλmax (MeOH) 336 nm (ε2,910), 323 (2,645), 297 (4,440), 286 (4,880), 236 (30,050), 224 (46,730).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04408077
Source datasetuspto-grants-1983_10
ORD IDord-57d685f0e7ee4cf4bd9f1d76a0b25571
Source noteuspto-grants-1983_10