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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980562Generated: October 30, 2026

2,6-Dimethylphenol → Phenol, 2,6-dimethyl-4-nitroso-

https://huagongshe.com/reaction/1980562

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DimethylphenolHCID 11335—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
ProductPhenol, 2,6-dimethyl-4-nitroso-HCID 83351—

Reaction Steps

25 Grams of 2,6-dimethylphenol was dissolved in 246 ml of 50% aqueous glacial acetic acid solution. To this solution being kept at 15° C. or lower was added dropwise 91 g of 30% aqueous sodium nitrite solution, whereby 2,6-dimethyl-p-nitrosophenol was obtained. The compound was reduced to be converted to an amino compound. The amino compound was subjected to diazotization at 0° to 2° C. Into the resulting reaction mixture was poured a 50% aqueous zinc chloride solution. By thorough mixing, a double salt of a diazonium salt with zinc chloride was deposited. Infrared absorption spectra (KBr tablet method): around 3300 cm-1, 2200 cm-1, 1570 cm-1, 1080 cm-1, 930 cm-1 ; ultraviolet absorption spectra (solvent: water), wavelength at maximum absorption: 364 nm. SYNTHESIS EXAMPLES 5 AND 6

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04510226
Source datasetuspto-grants-1985_04
ORD IDord-143e580dd7a347fdb2be88017a3b8a1b
Source noteuspto-grants-1985_04