HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579467Generated: October 26, 2026
Methanol → Ethyl 4-methoxy-3-oxobutanoate
https://huagongshe.com/reaction/579467
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Bromo-7-hydroxy-4-methylchromen-2-one | HCID 5337545 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | Ethyl 4-methoxy-3-oxobutanoate | HCID 12645099 | 15.1% |
Reaction Steps
NaH (7.71 g, 192.7 mmol) was suspended in DMF (110 mL). The solution of MeOH (2.64 g, 82.5 mmol) in DMF (55 mL) was added drop wise at 0° C. After that, the mixture was stirred at 0° C. for 30 min. The solution of compound 1 (9.54 g, 57.9 mmol) in DMF (55 mL) was added dropwise at 0° C., then the reaction mixture was allowed to warm slowly to RT and stirred for 16 h. The reaction mixture was diluted with 1N HCl (400 mL), extracted with MTBE (250 mL×3). The combined organic layer was washed with H2O (200 mL×5), dried over Na2SO4, filtered, concentrated, purified by silica gel column (PE:EA=10:1) afforded ethyl 4-methoxy-3-oxobutanoate (1.4 g, 15.1%) as light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09040714B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-9e7544d2fee74e90bb23995b25649632 |
|---|
| Source note | uspto-grants-2015_05 |
|---|