HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357804Generated: October 29, 2026
Methyl acetoacetate → HCID 54721729, compound
https://huagongshe.com/reaction/357804
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | 4-Methylbenzaldehyde | HCID 7725 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54721729 | HCID 54721729 | — |
Reaction Steps
The title compound was prepared as described in General Method 1 using 10 mL of methyl acetoacetate, 3.7 g of NaH 60% dispersion in oil, 58 mL of 1.6M n-butyl lithium in hexane, 10.9 mL of p-tolualdehyde and 250 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. 138°-139° C.). 1H NMR (CDCl3) δ 2.39 (s, 3 H), 2.93 (dd, 2 H), 3.58 (dd, 2 H), 5.69 (dd, 1 H), 7.23-7.31 (m, 4 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05840751 |
|---|
| Source dataset | uspto-grants-1998_11 |
|---|
| ORD ID | ord-112bcc48c32848ceb54e14cc20e3293b |
|---|
| Source note | uspto-grants-1998_11 |
|---|