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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493385Generated: October 30, 2026

Hydrochloric Acid → HCID 54915161, compound

https://huagongshe.com/reaction/493385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantBenzene, 1-nitro-3-phenoxy-HCID 69284—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon DisulfideHCID 6348—
SolventEthyl AcetateHCID 8857—
ProductHCID 54915161HCID 54915161—

Reaction Conditions

Temperature0 °C

Reaction Steps

The compound 1-nitro-3-phenoxybenzene (10.17 g, 0.0473 mol) is put into solution in carbon disulphide (70 ml). Aluminium chloride (10.06 g, 0.076 mol) is added by portions at ambient temperature. The reaction medium is cooled down to 0° C. then acetyl chloride (2.4 ml, 0.038 mol) is added dropwise. The reaction medium is left to return to 23° C. then stirring is maintained for 5 hours, followed by cooling down again to 0° C., then the careful addition of ethyl acetate, crushed ice and 3 N hydrochloric acid. After decantation, the medium is extracted with ethyl acetate. The organic phase is washed with water, with a saturated solution of sodium carbonate then with a saturated solution of sodium chloride. It is then dried over sodium sulphate then evaporated. The residue obtained is adsorbed on silica then purified by chromatography on a Biotage-type silica column (eluent: ethyl acetate-heptane: 1-4). After washing with diethyl ether, a yellow-coloured powder is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534805B2
Source datasetuspto-grants-2009_05
ORD IDord-e9b516c47f624b19b87cd08de2812c07
Source noteuspto-grants-2009_05