HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084880Generated: October 31, 2026
Methyl acetoacetate → HCID 86744710, compound
https://huagongshe.com/reaction/1084880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 20081800 | HCID 20081800 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 86744710 | HCID 86744710 | 96.2% |
Reaction Steps
82.2 μl (0.76 mmol) of methyl acetoacetate are added dropwise at 0° C. under a nitrogen atmosphere to 18.5 mg (0.8 mmol) of sodium hydride in 1 ml of tetrahydrofuran. After 15 minutes, 0.55 ml (0.77 mmol) of n-butylithium (1.5 M in hexane) is added dropwise at 0° C., the mixture is stirred for 15 minutes at 0° C. and 180 mg (0.7 mmol) of the compound from Example 31 are added dropwise in 3 ml of tetrahydrofuran. After 1 h, the mixture is hydrolyzed using saturated ammonium chloride solution and washed three times using dichloromethane, and the organic phases are dried and 0.25 g of oil are obtained after removing the solvent in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05006530 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-acf5eccde53e4428aa27b9107c8352b0 |
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| Source note | uspto-grants-1991_04 |
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