HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481839Generated: October 28, 2026
4-Chlorobenzaldehyde → HCID 54721559, compound
https://huagongshe.com/reaction/481839
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 54721559 | HCID 54721559 | — |
Reaction Steps
The title compound was prepared as described in General Method 1 using 10 mL of methyl acetoacetate, 3.9 g of NaH 60% dispersion in oil, 58 mL of 1.6M n-butyl lithium in hexane, 13.5 g of 4-chlorobenzaldehyde 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. 149°-150° C.). 'H NMR (CDCl3) δ2.83 (dd, 1H), 2.95 (dd, 1H), 3.60 (dd, 2H), 5.67 (dd, 1H), 7.33-7.44 (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-630331fe439e4286848098f154e19869 |
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| Source note | uspto-grants-1998_08 |
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