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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567224Generated: October 25, 2026

5-Methylcyclohexane-1,3-dione → 3-(3-Carbomethoxy-2-bromoanilino)-5-methyl-cyclohex-2-en-1-one

https://huagongshe.com/reaction/567224

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methylcyclohexane-1,3-dioneHCID 458095—
ReactantMethyl 3-amino-2-bromobenzoateHCID 13574117—
Product3-(3-Carbomethoxy-2-bromoanilino)-5-methyl-cyclohex-2-en-1-oneHCID 2274020267%

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of methyl 2-bromo-3-aminobenzoate (10.2 g, 44.3 mM) and 5-methyl-1,3-cyclohexanedione (6.15 g, 48.7 mm) was heated at 125° C. under a stream of nitrogen for 1.5 hours. The resultant solid was triturated with ethyl acetate to afford 9.98 g (67%) of 3-(3-carbomethoxy-2-bromoanilino)-5-methyl-cyclohex-2-en-1-one. 1H NMR (CDCl3) δ 7.55 (m, 2H), 7.35 (dd, J=8 and 8 Hz, 1H), 6.4 (bs, 1H), 5.55 (s, 1H), 3.95 (s, 3H), 2.6-2.0 (m, 5H), 1.15 (d, J=7 Hz, 3H). MS (ES) m/e 338, 340.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177440B1
Source datasetuspto-grants-2001_01
ORD IDord-edb1799688444ab7a105b77a716b82c0
Source noteuspto-grants-2001_01