HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975017Generated: October 29, 2026
Sodium Bicarbonate → Benzyl 2-(3-hydroxyprop-1-en-1-yl)pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/975017
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 53843982 | HCID 53843982 | — |
| Reactant | Phenylmethyl 2-(3-ethoxy-3-oxo-1-propen-1-yl)-1-piperidinecarboxylate | HCID 54132542 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl 2-(3-hydroxyprop-1-en-1-yl)pyrrolidine-1-carboxylate | HCID 4266884 | — |
| Product | 1-(N-benzyloxycarbonyl-piperid-2-yl)-3-hydroxypropene | HCID 54420541 | — |
Reaction Steps
To a stirred solution of either ethyl 3-(N-benzyloxycarbonylpyrrolidin-2-yl)-2-propenoate or ethyl-3-(N-benzyloxycarbonylpiperid-2-yl)-2-propenoate (R, or S, or racemate, 10.00 mmol) in anhydrous tetrahydrofuran (75 mL) at -78° C. under nitrogen was added dropwise a solution of diisobutylaluminium hydride (1.0M in hexanes, 12.0 mL, 22.0 mmol, 2.2 eq). The resulting solution was stirred at -78° C. under nitrogen for 30 minutes. The reaction solution was then allowed to warmed to room temperature over the course of 2 hours. A saturated solution of sodium hydrogen carbonate (50 mL) was added, and the aqueous mixture was extracted with ethyl acetate (3×50 mL). The extracts were combined, dried (MgSO4), and evaporated under reduced pressure. Column chromatography of the residue with diethyl ether/hexanes [1:1] afforded either 1-(N-benzyloxycarbonylpyrrolidin-2-yl)-3-hydroxypropene or 1-(N-benzyloxycarbonyl-piperid-2-yl)-3-hydroxypropene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05607951 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-cc67781cb23345f69fa801283cf75952 |
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| Source note | uspto-grants-1997_03 |
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