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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16609Generated: October 29, 2026

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

https://huagongshe.com/reaction/16609

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 numberUS07737163B2
Source datasetuspto-grants-2010_06
ORD IDord-a4ae0e0299e042ff87863631cd2d1504
Source noteuspto-grants-2010_06