HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481841Generated: October 30, 2026
Methyl acetoacetate → HCID 54721661, compound
https://huagongshe.com/reaction/481841
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzaldehyde, 4-(phenylmethoxy)- | HCID 78109 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 54721661 | HCID 54721661 | — |
Reaction Steps
The title compound was prepared as described in General Method 1 using 5.0 mL of methyl acetoacetate, 2.0 g of NaH 60% dispersion in oil, 25 mL of 2.0M n-butyl lithium in hexane, 12.0 g of 4-benzyloxybenzaldehyde and 150 mL of tetrahydrofuran. After addition of the aldehyde, the reaction was stirred for 15 minutes at 0° C. then allowed to warm to room temperature overnight. The crude product was triturated from diethyl ether to afford a solid (m.p. 165°-166° C.). 'H NMR (CDCl3) δ2.91 (dd, 2H), 3.56 (dd, 2H), 5.09 (s, 2H), 5.65 (dd, 1H), 6.98-7.04 (m, 2H), 7.30-7.44 (m, 7H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05789440 |
|---|
| Source dataset | uspto-grants-1998_08 |
|---|
| ORD ID | ord-0e85ff008965489ab9059ce7d8670248 |
|---|
| Source note | uspto-grants-1998_08 |
|---|