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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Methylcyclohexane-1,3-dione | HCID 458095 | — |
| Reactant | Methyl 3-amino-2-bromobenzoate | HCID 13574117 | — |
| Product | 3-(3-Carbomethoxy-2-bromoanilino)-5-methyl-cyclohex-2-en-1-one | HCID 22740202 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06177440B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-edb1799688444ab7a105b77a716b82c0 |
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| Source note | uspto-grants-2001_01 |
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