HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488668Generated: October 26, 2026
Trichloroacetic Acid → 8-Methoxy-2,3,4,5-tetrahydro-benzo[c]azepin-1-one
https://huagongshe.com/reaction/1488668
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trichloroacetic Acid | HCID 6421 | — |
| Reactant | 7-Methoxy-1-tetralone Oxime | HCID 57371006 | — |
| Product | 8-Methoxy-2,3,4,5-tetrahydro-benzo[c]azepin-1-one | HCID 11275529 | 22.3% |
Reaction Steps
Following a procedure of Tomita, et. al., H. Chem. Soc. C1969, 183, 7-methoxytetralone oxime (45.0 g, 0.235 mol) was mixed with solid trichloroacetic acid (150 g), and the resulting suspension heated to ca. 80 C. at which time a violent exotherm ensued, yielding a black solid mixture. The residue was cooled, partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution, and the combined organic layers were concentrated in vacuo. The residue was purified by chromatography over silica gel to yield 10.0 g (22%) of 8-methoxy-2,3,4,5-tetrahydro-1H-2-benzazepin-1-one. An analytical sample was obtained by recrystallization from CH2Cl2 /hexanes to yield colorless crystals: mp. 99°-101° C. (lit. (see above) 100°-101° C.); 1H NMR(CDCl3) d7.35(brs, 1H), 7.30(d, J=3 Hz, 1H), 7.10(d, J=9 Hz, 1H), 6.95(dd, J=3, 9 Hz, 1H), 3.82(s, 3H), 3.10(q, J=6 Hz, 2H), 2.80(b, J=6 Hz, 2H), 1.98 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05674865 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-4eb53c4171a34b4789679f3d247bd836 |
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| Source note | uspto-grants-1997_10 |
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