HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408825Generated: November 1, 2026
Ethyl bromoacetate → HCID 67359342, compound
https://huagongshe.com/reaction/2408825
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 3,3-Diphenyl-3,4,5,6-tetrahydropyridin-2-ol | HCID 321165 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67359342 | HCID 67359342 | — |
Reaction Steps
To a solution of the product of Example 1C (2.51 g, 10.00 mmol) in tetrahydrofuran (100 mL) was added potassium tert-butoxide (1.35 g, 12.00 mmol) under nitrogen followed by ethyl 2-bromoacetate (1.22 mL, 11.00 mmol). The reaction mixture was heated to 80° C. and stirred overnight. The reaction mixture was cooled to room temperature, concentrated and then diluted with ethyl acetate. The organic layer was washed with water and brine, dried over magnesium sulfate, filtered and concentrated. Silica gel chromatography eluting with ethyl acetate/hexane (20:80) gave the title compound. MS (DCI+) m/z 338 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815869B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-c6e3b4b0a5b84eab904c8fb4a451cc58 |
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| Source note | uspto-grants-2014_08 |
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