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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887393Generated: October 31, 2026

Acetate → HCID 12732179, compound

https://huagongshe.com/reaction/887393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantRiboflavinHCID 493570—
ReactantHCID 10554200HCID 10554200—
SolventMethanolHCID 887—
ProductHCID 12732179HCID 12732179—

Reaction Steps

To a solution of (S)-2-(1-benzylpyrrolidin-2-yl)propan-2-ol (1.38 g, 6.29 mmol) in MeOH (50 mL) was added palladium hydroxide, 20 wt % pd (dry basis) on carbon, wet, degussa type e101 ne/w (230 mg, 1.64 mmol) and acetic acid glacial (690 μl, 12.0 mmol). The reaction mixture was stirred at RT under 1 atm of H2 for 24 h. The reaction mixture was filtered through a pad of celite and washed with MeOH. The solvent was evaporated and the residue was partitioned between 2 N NaOH and EtOAc. The aqueous layer was extracted with EtOAc (2×) and the combined organic layer was dried (Na2SO4) and concentrated. The crude product was chromatographed through a Redi-Sep® pre-packed silica gel column (40 g), eluting with a gradient of 50% to 100% MeOH in EtOAc, to provide (S)-2-(pyrrolidin-2-yl)propan-2-ol as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247418B2
Source datasetuspto-grants-2012_08
ORD IDord-fafbc54ce9524077af4dcd37ce1486bc
Source noteuspto-grants-2012_08