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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896010Generated: October 25, 2026

Boron trifluoride etherate → tert-Butyl 4-hydroxy-4-(3-phenylprop-2-ynyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1896010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantLithium phenylacetylideHCID 3437284—
Reactanttert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-hydroxy-4-(3-phenylprop-2-ynyl)piperidine-1-carboxylateHCID 8662734691.9%

Reaction Conditions

Temperature-75 °C

Reaction Steps

Boron trifluoride diethyl etherate (0.131 mL, 1.03 mmol) followed by lithium phenylacetylide (1M in THF, 1.03 mL, 1.03 mmol) was dropped into a solution of Compound 256a (200 mg, 0.938 mmol) in THF (5 mL) stirred at −75° C. under nitrogen atmosphere. Stirring and cooling were kept on for 2 h and after overnight stirring at r.t., the reaction mixture was quenched with water and EtOAc. The combined extracts were washed, dried over Na2SO4 and evaporated to dryness. The residue was purified by flash chromatography (EtOAc—Petroleum Ether 85:15) affording the title product (272 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518916B2
Source datasetuspto-grants-2013_08
ORD IDord-aad17222f93344df9a3fc42be36177bf
Source noteuspto-grants-2013_08