HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453758Generated: October 29, 2026
Ethyl bromoacetate → HCID 25175166, compound
https://huagongshe.com/reaction/453758
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 1106938-11-7 | HCID 25175001 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 25175166 | HCID 25175166 | 71.5% |
Reaction Steps
To a solution of (R*)-3-{1-[(S)-1-(2,3-dihydrobenzo[1,4]dioxin-2-yl)methyl]piperidin-3-yl}phenol (201 mg, 0.62 mmol) in dry DMF (2 ml) was added NaH (60% in oil, 30 mg, 0.75 mmol) under nitrogen atmosphere and the mixture was stirred at 0° C. for 5 min, then allowed to warm to RT and stirred for further 2.5 h. The reaction mixture was cooled to 0° C., ethyl bromoacetate (106 mg, 0.62 mmol) was added and the mixture was stirred at RT overnight. Potassium tert-butoxide (69 mg, 0.61 mmol) was added and the mixture was stirred for 3 h at RT and filtered. The precipitate was dissolved in dry MeOH, the solution filtered and evaporated to dryness to give 170 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492549B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-8fd8156a901042cc8cdeb8718fe1d523 |
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| Source note | uspto-grants-2013_07 |
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