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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198834Generated: November 4, 2026

Sulfuric Acid → Phenol, 4-(5-octyl-2-pyridinyl)-

https://huagongshe.com/reaction/1198834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 19867286HCID 19867286—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductPhenol, 4-(5-octyl-2-pyridinyl)-HCID 172548435.2%

Reaction Conditions

Temperature5 °C

Reaction Steps

10 ml of 3N sulphuric acid were treated while stirring with 1.8 g of p-(5-octyl-2-pyridyl)aniline. The mixture was cooled to 5° C. and then treated dropwise at 0°-5° C. within about 3 minutes with a solution of 0.442 g of sodium nitrite in 2 ml of water. The brown mixture obtained was poured into 100 ml of water and heated to reflux for 30 minutes while stirring. The reaction mixture was subsequently cooled to room temperature, adjusted to about pH 5 with 7 ml of 3N sodium hydroxide solution and extracted once with 200 ml of methylene chloride and once with 100 ml of methylene chloride. The organic phases were washed with 150 ml of dilute sodium chloride solution, dried over sodium sulphate and evaporated in a vacuum. The residue (1.867 g) was separated by chromatography on 250 g of silica gel at 0.4 bar with methylene chloride and methylene chloride/acetone. Recrystallization of the resulting red-brown oil in diethyl ether/hexane at 0° C. gave 0.635 g of p-(5-octyl-2-pyridyl)phenol as beige crystals. Working-up of the mother liquor gave 0.355 g of crude p-(5-octyl-2-pyridyl)phenol as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04898455
Source datasetuspto-grants-1990_02
ORD IDord-160964ccfb6147fd93e64d94f8c58491
Source noteuspto-grants-1990_02