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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16218Generated: October 29, 2026

Tetrabutylammonium Fluoride → 1-(5-Hydroxy-cyclooctyl)-4-hydroxymethyl-3,3-dimethyl-pyrrolidin-2-one

https://huagongshe.com/reaction/16218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 131727099HCID 131727099—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Hydroxy-cyclooctyl)-4-hydroxymethyl-3,3-dimethyl-pyrrolidin-2-oneHCID 66665275—

Reaction Steps

Tetrabutyl ammonium fluoride (0.76 mL, 1 M in tetrahydrofuran, 0.76 mmol) was added to a stirred solution of the product of Example 5J (0.30 g, 0.60 mmol) in tetrahydrofuran (5 mL) at room temperature. The resulting solution was stirred for two hours and then partitioned with ethyl acetate and water. The organic phase was washed with brine, dried (MgSO4), filtered, and evaporated. The residue was purified over silica gel using 20-100% ethyl acetate in hexanes to give the titled product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737137B2
Source datasetuspto-grants-2010_06
ORD IDord-8012f60afd3942c4875f0b33cff45857
Source noteuspto-grants-2010_06