HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl acetoacetate → HCID 54676620, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 69836228 | HCID 69836228 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 54676620 | HCID 54676620 | — |
| Product | HCID 69836228 | HCID 69836228 | — |
Reaction Steps
The title compound was prepared as described in General Method 1 using 25 mmol of methyl acetoacetate, 27.5 mmol of NaH 60% dispersion in oil, 26.25 mmol of 1.6M n-butyl lithium in hexane in 50 mL of tetrahydrofuran and 25 mmol of 3-benzoylpropionic acid sodium salt in 60 mL of tetrahydrofuran. 3-Benzoylpropionic acid sodium salt was prepared by reacting the acid (25 mmol) with hexane washed NaH (26.25 mmol) in tetrahydrofuran at 0° C. for 30 minutes. The crude product was flash chromatographed using CH2Cl2 /MeOH/CH3CO2H (90/10/0.2) to give a viscous gum. 1H NMR (CDCl3) δ2.1-2.6 (m, 4H), 2.9 (d, 1H), 3.0 (d, 1H), 3.3 (d, 1H), 3.4 (d, 1H), 7.2-7.5 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05789440 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-d907971ea4c44e6e959cfa117cadf189 |
| Source note | uspto-grants-1998_08 |