HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458454Generated: October 30, 2026
Hexanoic Acid → ETHYL 7-METHYL-3-OXOOCTANOATE
https://huagongshe.com/reaction/458454
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexanoic Acid | HCID 8892 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ETHYL 7-METHYL-3-OXOOCTANOATE | HCID 10821911 | 99% |
Reaction Steps
To a stirred solution of Meldrum's Acid (2.0 g, 13.9 mmol) in 100 mL of CH2Cl2, hexanoic acid (1.61 g, 13.9 mmol) was added followed by DMAP (3.39 g, 27.8 mmol) and finally DCC (2.86 g, 13.9 mmol). The reaction stirred overnight at room temperature. The mixture was then filtered and the filtrate washed with 1M HCl, H2O and Brine. The organics were then dried over sodium sulfate, filtered and concentrated to a yellow oil. The material was then dissolved in 100 mL of EtOH and refluxed overnight. The reaction mixture was concentrated to yield 2.58 g (99%) of a clear oil. No purification performed: 1H NMR (CDCl3, 400 MHz) δ 4.22–4.12 (q, 2H, J=7.07), 3.40 (s, 2H), 2.56–2.44 (t, 2H, J=7.42), 1.69–1.43 (m, 3H), 1.30–1.21 (t, 3H, J=7.07), 1.19–1.09 (m, 2H), 0.89–0.81 (d, 6H, J=6.55).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07189851B2 |
|---|
| Source dataset | uspto-grants-2007_03 |
|---|
| ORD ID | ord-fc0478a1d9ec421b8a7f3c513b4ad7ef |
|---|
| Source note | uspto-grants-2007_03 |
|---|