HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → Methyl 4-amino-5-butyryl-1-hydroxycyclohexa-2,4-diene-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 1-Hexen-3-one | HCID 15395 | — |
| Reactant | Methyl 5-aminofuran-2-carboxylate | HCID 5072225 | — |
| Product | Methyl 4-amino-5-butyryl-1-hydroxycyclohexa-2,4-diene-1-carboxylate | HCID 21086195 | — |
Reaction Steps
A stirred solution of methyl 5-amino-2-furoate (1.4 g, 10 mmol) and 1-hexen-3-one (7 mL, 60 mmol) in benzene (50 mL) was heated to reflux for 2 h. The reaction mixture was concentrated under reduced pressure to afford a crude oil. Purification by flash column chromatography (silica, 2:1 hexanes/ethyl acetate) provided methyl 4-amino-5-butyryl-1-hydroxycyclohexa-2,4-diene-1-carboxylate (1.25 g): 1H NMR (300 MHz, CDCl3): δ 6.26–6.23 (m, 1H), 6.09–6.05 (m, 1H), 3.80 (s, 3H), 3.02–2.96 (m, 1H), 2.89–2.84 (m, 1H), 2.42–2.37 (m, 2H) 1.64–1.57 (m, 2H), 0.96–0.88 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07176242B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-8150968c79d2423c81034c50f5e7b8fd |
| Source note | uspto-grants-2007_02 |