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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106286Generated: October 31, 2026

Toluene → 1-(3-amino-4-chlorophenyl)ethanone

https://huagongshe.com/reaction/1106286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
ReactantStannous chloride dihydrateHCID 61436—
Reactant4'-Chloro-3'-nitroacetophenoneHCID 79596—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
Product1-(3-amino-4-chlorophenyl)ethanoneHCID 277832587.5%

Reaction Steps

A mixture of 39.8 g of 4-chloro-3-nitroacetophenone and 136 g of SnCl2.2H2O in 220 ml of concentrated HCl is stirred at room temperature for 0.5 hours. The reaction mixture warms spontaneously to 70° C. then cools. Toluene (200 ml) is added and the reaction mixture is made alkaline with 30% NaOH. Ether is added and the layers are separated. The aqueous layer is extracted twice more with ether, the organic layers are combined, dried, and evaporated. The solid residue is crystallized from benzene to yield 29.6 g of the title compound, melting point 104°-105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04312990
Source datasetuspto-grants-1982_01
ORD IDord-dabe65c3516b4de2a373772155b49dc9
Source noteuspto-grants-1982_01