HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721461Generated: November 4, 2026
Acetone → Methyl 2-methylazulene-1-carboxylate
https://huagongshe.com/reaction/1721461
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | 3-(Methoxycarbonyl)-2H-cyclohepta[b]furan-2-one | HCID 10081616 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 2-methylazulene-1-carboxylate | HCID 11264110 | — |
Reaction Steps
2-Methylazulene was synthesized according to a method described in Japanese Patent Laid-Open Publication No. 207232/1987. Specifically, 19.5 g (0.16 mol) of tropolone was reacted with 40 g (0.21 mol) of p-toluenesulfonic acid chloride in pyridine to give 37.1 g of tosylated tropolone. Then, 20 g (0.15 mol) of dimethylmalonate was reacted with 9.7 g (0.18 mol) of NaOMe in methanol at room temperature for 4 hr to give 14.4 g of 3-methoxycarbonyl-2H-cyclohepta(b) furan-2-one (Compound (2)). Then, 12 g of Compound (2), 200 ml of acetone and 70 ml of diethylamine were added, and the mixture was heated under reflux for 30 hr. Thereafter, H2O was added thereto, and the mixture was extracted with toluene to give 39.2 g of methyl-2-methylazulene carboxylate. Further, 25 ml of phosphoric acid was added, and a reaction was allowed to proceed at 85° to 90° C. for one hr. The reaction mixture was decomposed with water, extracted with benzene and dried to give 6.5 g of 2-methylazulene as an intended product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05510502 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-5c7093494559404f8ca1135715b75507 |
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| Source note | uspto-grants-1996_04 |
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