HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481840Generated: October 30, 2026
Methyl acetoacetate → HCID 54721671, compound
https://huagongshe.com/reaction/481840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | 3-Chlorobenzaldehyde | HCID 11477 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 54721671 | HCID 54721671 | — |
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, 6.5 mL of 3-chlorobenzaldehyde 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. 122°-124° C.). 'H NMR (CDCl3) δ2.83 (dd, 1H), 2.96 (dd, 1H), 3.60 (dd, 2H), 5.68 (dd, 1H), 7.25-7.42 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05789440 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-9d2caf249123429c8a65dad13cdd2e7c |
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| Source note | uspto-grants-1998_08 |
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