HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323497Generated: October 26, 2026
Hydrogen Peroxide → 1-(3,4,5-Trimethoxybenzyl)-3-(4-fluorophenylmethyl)-3-(3-hydroxypropyl)-2-oxopyrrolidine
https://huagongshe.com/reaction/323497
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| Reactant | 1-(3,4,5-Trimethoxybenzyl)-3-(4-fluorophenylmethyl)-3-(allyl)-2-oxopyrrolidine | HCID 22009333 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 1-(3,4,5-Trimethoxybenzyl)-3-(4-fluorophenylmethyl)-3-(3-hydroxypropyl)-2-oxopyrrolidine | HCID 18464480 | — |
Reaction Steps
Combine 1-(3,4,5-trimethoxybenzyl)-3-(4-fluorophenylmethyl)-3-(allyl)-2-oxopyrrolidine (0.677 g, 1.64 mmol) and tetrahydrofuran (10 mL). Add dropwise a solution of 9-BBN (9-borabicyclo[3.3.1]nonane) (5.56 mL, 0.5 M, 2.78 mmol) in tetrahydrofuran. After 1.5 hours, add dropwise an aqueous sodium hydroxide solution (10 mL, 1 M) and 30% aqueous hydrogen peroxide (1.5 mL, about 14.7 mmol). After 15 minutes heat the reaction mixture to reflux. After 1 hour, cool to ambient temperature, saturate the aqueous mixture with potassium carbonate and separate the layers. Extract the aqueous layer five times with diethyl ether. Combine the organic layers and dry over potassium carbonate, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 5% methanol/dichloromethane to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211199B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-e0fe1c64531a4978b2bce8b2f5d10326 |
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| Source note | uspto-grants-2001_04 |
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