HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450082Generated: October 26, 2026
Hydrochloric Acid → 1-(2-Methoxy-5-nitrophenyl)ethanone
https://huagongshe.com/reaction/450082
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Reactant | 2-Methoxy-5-nitro-benzoyl chloride | HCID 13719593 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | (Methanesulfinyl)methane--water (1/1) | HCID 23503278 | — |
| Product | 1-(2-Methoxy-5-nitrophenyl)ethanone | HCID 18615104 | 78% |
Reaction Steps
Anhydrous magnesium chloride (150 mg, 1.6 mmol) was added to a solution of diethyl malonate (440 mg, 2.76 mmol) and triethylamine (670 mg, 6.5 mmol) in dry toluene (10 ml) at room temperature under inert atmosphere. After stirring for 1 hr, the reaction was cooled to 0° C. and 2-methoxy-5-nitro benzoyl chloride (550 mg, 2.3 mmol) was added. The reaction mixture was allowed to attain room temperature then stirred for 30 min before adding 6N hydrochloric acid (15 ml). The organic layer was separated, washed with water and dried. Concentration under reduced pressure gave a residue to which was added 1:1 DMSO-water (10 ml). The mixture was heated to 140° C. for 2 hr, then cooled to RT and diluted with ethyl acetate (50 ml). The organic layer was washed successively with water, bicarbonate solution, and brine, then dried. Evaporation under reduced pressure gave 1-(2-Methoxy-5-nitro-phenyl)-ethanone (350 mg, 70%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486962B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-3778d97583ef4936883c6eb78a5a126c |
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| Source note | uspto-grants-2013_07 |
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