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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256066Generated: November 2, 2026

2-Fluoropyridine → benzyl 4-(2-fluoropyridin-3-yl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/2256066

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoropyridineHCID 9746—
ReactantLithium BromideHCID 82050—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
ReactantLithium diisopropylamideHCID 2724682—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Productbenzyl 4-(2-fluoropyridin-3-yl)-4-hydroxypiperidine-1-carboxylateHCID 12016071—

Reaction Conditions

Temperature-50 °C

Reaction Steps

To a solution of lithium diisopropylamide (0.31 mol) in 300 mL of anhydrous tetrahydrofuran:hexane at -78° C. was added a solution of 2-fluoropyridine (24.6 mL) in 40 mL of anhydrous tetrahydrofuran. The reaction mixture was allowed to warm to -50° C., cooled back to -74° C. and treated dropwise with a solution of lithium bromide (55.5 g) and 1-benzyloxycarbonyl-4-oxopiperidine (55.5 g) in 300 mL of anhydrous tetrahydrofuran so that the temperature of the reaction mixture remained below -70° C. After the addition was complete, the reaction mixture was allowed to warm to -30° C. and then treated with water. The organic layer was separated and the aqueous layer was extracted with two portions of ether. Combined organic layers were dried and evaporated to afford the crude product. This material was purified by column chromatography to afford the pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654299
Source datasetuspto-grants-1997_08
ORD IDord-18d71a69368e48e4b1b44523334e0e52
Source noteuspto-grants-1997_08