HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66459Generated: October 25, 2026
Hydrochloric Acid → 1-(3,4-Dimethoxyphenyl)-7-(4-methoxyphenyl)-2-nitro-5-heptanone
https://huagongshe.com/reaction/66459
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzene, 1,2-dimethoxy-4-(2-nitroethyl)- | HCID 10036050 | — |
| Reactant | 1-Iodo-5-(4-methoxyphenyl)-3-pentanone | HCID 13065019 | — |
| Reactant | Nitro ketone | HCID 54223030 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3,4-Dimethoxyphenyl)-7-(4-methoxyphenyl)-2-nitro-5-heptanone | HCID 13065020 | — |
Reaction Steps
To a solution of 15 g. (0.071 mole) of 2-(3,4-dimethoxyphenyl)-1-nitroethane in 200 ml. of dry tetrahydrofuran was added 33.45 g. (0.08 mole) of 40% Triton B at room temperature. The solution was stirred at room temperature for 14 minutes under N2. 22.6 g. (0.071 mole) of 1-iodo-5-(4-methoxyphenyl)-3-pentanone was then added in portions. The mixture was heated at 50°-55° for 2 hours under N2 until no more starting material was detected on TLC, and then cooled to room temperature. The resulting reaction solution was poured into cold dil. HCl and extracted with ethyl acetate. The organic layer was dried over anhydrous MgSO4. The crude material was chromatographed on Florisil to provide 22 g. of desired nitro ketone derivative. Recrystallization from 80% ethanol gave a white solid which has m.p. 87°-89° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04342692 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-3f5f0db0de82463591055f422ac4d9a0 |
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| Source note | uspto-grants-1982_08 |
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