Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655692Generated: October 27, 2026

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

https://huagongshe.com/reaction/1655692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetic AcidHCID 6421—
Reactant7-Methoxy-1-tetralone OximeHCID 57371006—
Product8-Methoxy-2,3,4,5-tetrahydro-benzo[c]azepin-1-oneHCID 1127552922.3%

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 numberUS05250679
Source datasetuspto-grants-1993_10
ORD IDord-28f9809a9f6f410f845a1ecb7413426a
Source noteuspto-grants-1993_10