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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615519Generated: October 29, 2026

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

https://huagongshe.com/reaction/615519

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) 67 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 (ε 2,910), 323 (2,645), 297 (4,440), 286 (4,880), 236 (30,050), 224 (46,730).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04499310
Source datasetuspto-grants-1985_02
ORD IDord-fdf936f284b24136ab501a579d9ec4c4
Source noteuspto-grants-1985_02