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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164638Generated: November 1, 2026

Sulfuric Acid → Benzonitrile, 2-(3,4-dichlorophenoxy)-5-(methylsulfonyl)-

https://huagongshe.com/reaction/2164638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium CyanideHCID 8929—
ReactantBenzenamine, 2-(3,4-dichlorophenoxy)-5-(methylsulfonyl)-HCID 514872—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductBenzonitrile, 2-(3,4-dichlorophenoxy)-5-(methylsulfonyl)-HCID 51486896.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 5.0 g (0.0151 mole) of 2-(3,4-dichlorophenoxy)-5-(methylsulfonyl)benzenamine (Example 16), 75 ml of glacial acetic acid, 37.5 ml of water and 3.0 g (0.0306 mole) of concentrated sulfuric acid was cooled to 0° C. and 1.5 g (0.0217 mole) of sodium nitrite dissolved in 15 ml of water was added slowly. The mixture was stirred at 0° C. for 20 minutes and then added slowly to a mixture of 7.5 g (0.0838 mole) of cuprous cyanide and 30 g (0.612 mole) of sodium cyanide dissolved in 150 ml of water at 0° C. The mixture was stirred at 0° C. for 45 minutes and allowed to warm to room temperature. The mixture was then heated at 50° C. for 1 hr. The mixture was poured into water and the crystalline product collected by filtration, washed with water and dried, to obtain 4.95 g (96.1% yield) of product. Purification was accomplished by column chromatography using silica gel as the support and chloroform as the eluent followed by recrystallization from ethyl acetate, which gave purified 2-(3,4-dichlorophenoxy)-5-(methylsulfonyl)benzonitrile, mp 162°-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04505929
Source datasetuspto-grants-1985_03
ORD IDord-01ee7284c7044bcd86cf3a8dde942360
Source noteuspto-grants-1985_03