HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493385Generated: October 30, 2026
Hydrochloric Acid → HCID 54915161, compound
https://huagongshe.com/reaction/493385
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Benzene, 1-nitro-3-phenoxy- | HCID 69284 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54915161 | HCID 54915161 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534805B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-e9b516c47f624b19b87cd08de2812c07 |
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| Source note | uspto-grants-2009_05 |
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