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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736428Generated: October 29, 2026

Water → tert-Butyl [(4-fluoropiperidin-4-yl)methyl]carbamate

https://huagongshe.com/reaction/736428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantN-benzoyl-4-tert-butoxycarbonylaminomethyl-4-fluoropiperidineHCID 67231354—
SolventEthanolHCID 702—
Producttert-Butyl [(4-fluoropiperidin-4-yl)methyl]carbamateHCID 5341522658.2%

Reaction Steps

A mixture of N-benzoyl-4-tert-butoxycarbonylaminomethyl-4-fluoropiperidine (step 3 of Example 15) (4.42 g, 13.1 mmol), NaOH (2.62 g, 65.5 mmol), H2O (9.00 mL) and ethanol (90.0 mL) was refluxed for 15 h and concentrated in vacuo. To the resulting residue were added water and chloroform. The organic layer was separated, dried over magnesium sulfate, and concentrated under reduced pressure. Recrystallization of the resulting solid with hexane-CH2Cl2 afforded a colorless solid 1.77 g (58%) as the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595329B2
Source datasetuspto-grants-2009_09
ORD IDord-f114882aac1c47acbf27acabde07ac00
Source noteuspto-grants-2009_09