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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865334Generated: October 25, 2026

Trichloroacetic Acid → 8-Methoxy-2,3,4,5-tetrahydro-benzo[c]azepin-1-one

https://huagongshe.com/reaction/865334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetic AcidHCID 6421—
ReactantHCID 57371006HCID 57371006—
Product8-Methoxy-2,3,4,5-tetrahydro-benzo[c]azepin-1-oneHCID 1127552922.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

Following a procedure of Tomita, et. al., J. Chem. Soc. C 1969, 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(t, J=6 Hz, 2H), 1.98(m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565449
Source datasetuspto-grants-1996_10
ORD IDord-7a9a7c49b62948488e3e3a30820ded4f
Source noteuspto-grants-1996_10