HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212558Generated: October 25, 2026
Diethyl dimethylmalonate → 3-(4-Benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl ester
https://huagongshe.com/reaction/2212558
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl dimethylmalonate | HCID 15382 | — |
| Reactant | 1-Bromo-4-phenylmethoxybenzene | HCID 138835 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl ester | HCID 69596508 | 50.4% |
Reaction Steps
sec-Butyl lithium (5.85 mL, 7.6 mmol) was added to a solution of 1-bromo-4-benzyloxy-benzene (2.0 g, 7.6 mmol) in THF (10 mL) cooled to −78° C. under nitrogen. The reaction was stirred for 1 h and diethyl dimethylmalonate (4.29 g, 22.8 mmol) was added rapidly. This was stirred for an additional 0.5 h and then allowed to warm to room temperature. The reaction was partitioned between ethyl acetate and 1 N HCl. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated to give an oil. The product was purified by flash column chromatography (FCC) on silica gel eluting hexane:ethyl acetate (90: 10, v:v) to give 3-(4-benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl ester (1.25 g, 50%) as an oil. MS found: (M+H)+=327.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07102008B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-5359d81de4724a08af69adbf01961d95 |
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| Source note | uspto-grants-2006_09 |
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