HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366957Generated: October 26, 2026
Methyl acetoacetate → Methyl 3-oxo-5-(phenylthio)pentanoate
https://huagongshe.com/reaction/366957
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chlorophenyl methyl sulfide | HCID 2737363 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tetrahydrofuran HMPA | HCID 86583969 | — |
| Product | Methyl 3-oxo-5-(phenylthio)pentanoate | HCID 12764772 | 22.7% |
Reaction Steps
To a suspension of NaH (60%) (815 mg, 20.39 mmol) in THF-HMPA (20 ml, 5 ml) was added methylacetoacetate (2.0 g, 18.5 mmol) in THF (5 ml) at 0° C. The mixture was stirred for 10 min. at 0° C. under nitrogen atmosphere. BuLi (12.3 ml, 20.39 mmol) was dropwise added and the red mixture was stirred for 15 min. at 0° C. Then a solution of chlorothioanisole (2.7 ml, 20.39 mmol) in THF (5 ml) was added to the mixture at 0° C. The mixture was stirred for 1 h at -5° C. The mixture was quenched with H2O, then extracted with AcOEt (100 ml×2). AcOEt layer was washed with H2O (10 ml×2) and brine (10 ml), then dried over MgSO4 and evaporated. The residue was purified by a silica gel column chromatography (150 g, hexane :AcOEt=6:1) to give a colorless oil (1.0 g, 22.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06131226 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-0662be53814b40eda18d24f9bf08d60d |
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| Source note | uspto-grants-2000_10 |
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