HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567259Generated: October 26, 2026
1,3-Cyclohexanedione → 3-(3-Carbomethoxy-2-bromoanilino)cyclohex-2-en-1-one
https://huagongshe.com/reaction/567259
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | Methyl 3-amino-2-bromobenzoate | HCID 13574117 | — |
| Product | 3-(3-Carbomethoxy-2-bromoanilino)cyclohex-2-en-1-one | HCID 22337724 | 92.5% |
Reaction Steps
A mixture of methyl 2-bromo-3-aminobenzoate (13.2 g, 60.0 mM) and 1,3-cyclohexanedione (8.4 g, 75 mM) was heated at 125° C. under a stream of nitrogen for 4 h. The resultant solid was purified by HPLC on silica gel (elution with methylene chloride/ethyl acetate) to afford 17.2 g (88%) of 3-(3-carbomethoxy-2-bromoanilino)cyclohex-2-en-1-one as a tan foam. 1H NMR (DMSO-d6) δ 8.75 (s, 1H), 7.6-7.4 (m, 3H), 4.65 (s, 1H), 3.85 (s, 3H), 2.6 (t, 2H, J=6 Hz), 2.15 (t, 2H, J=6 Hz), and 1.9 (m, 2H). IR (CHCl3, cm−1) 3400, 3004, 2954, 1732, 1607, 1588, 1573, 1513, 1464, 1436, 1412, 1308, 1249, 1177, and 1144. MS (ES) m/e 322, 324, 326.
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-88b9b4b7b2574a81a24bbcef012c2a65 |
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| Source note | uspto-grants-2001_01 |
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