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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612795Generated: October 31, 2026

Benzonitrile, 2-(3,4-dichlorophenoxy)- → HCID 19926666, compound

https://huagongshe.com/reaction/1612795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrile, 2-(3,4-dichlorophenoxy)-HCID 514863—
ReactantSodium BicarbonateHCID 516892—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
ProductHCID 19926666HCID 1992666675%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 10 g of anhydrous aluminum chloride in 150 ml of dry diethyl ether was added dropwise under nitrogen to a suspension of 3.1 g of lithium aluminum hydride in 150 ml of dry diethyl ether, and the mixture was cooled at 0° C. After 30 min at 0° C., a solution of 5.0 g of 2-(3,4-dichlorophenoxy)benzonitrile in 150 ml of dry diethyl ether was added slowly. The mixture was stirred for 24 h at 25° C., and a concentrated aqueous solution of sodium hydrogen carbonate was added. The precipitate was filtered off, the filtrate was evaporated to dryness, dissolved in ethyl acetate, and acidified with a concentrated solution of hydrochloric acid in ethanol. The precipitate was collected and recrystallized from a mixture of ethanol and diethyl ether, to give in 75% yield 2-(3,4-dichlorophenoxy)benzenemethanamine hydrochloride. mp 213° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05190965
Source datasetuspto-grants-1993_03
ORD IDord-56d8f63501e34337863efb1030ad59e9
Source noteuspto-grants-1993_03