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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770116Generated: November 1, 2026

1,2-Dichloroethane → 6-Chloro-1-phenyl-1-hexanone

https://huagongshe.com/reaction/1770116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
Reactant(4-Chlorobutyl)benzeneHCID 78543—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
Product6-Chloro-1-phenyl-1-hexanoneHCID 4182730—

Reaction Steps

To a 250 ml round-bottomed flask were added 5.0 g (29.65 mmol) 1-chloro-4-phenylbutane and 10 ml 1,2-dichloroethane. To the stirred solution was added a solution of 4.35 g (32.62 mmol) aluminum chloride and 4.22 ml (59.31 mmol) acetyl chloride in 50 ml 1,2-dichloroethane. The solution evolved HCl as it was stirred at room temperature for 1 hour. It was then poured into water, the layers separated, and the organic layer washed with 1N HCl, aqueous sodium bicarbonate solution, brine, dried over sodium sulfate, and evaporated to an oil, 6.7 g (>100%). NMR (delta, CDCl3): 1.76 (m, 4H), ~2.5 (s, 3H), 3.50 (m, 2H), 7.2 and 7.85 (m, 4H). IR cm-1, neat): 1678 (C =O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05385916
Source datasetuspto-grants-1995_01
ORD IDord-29b9ee8e8b8a4db6a3ba2d89b065938b
Source noteuspto-grants-1995_01