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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899728Generated: October 30, 2026

Methyl morpholine oxide → tert-Butyl 2-formylpiperidine-1-carboxylate

https://huagongshe.com/reaction/899728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl morpholine oxideHCID 82029—
ReactantN-Boc-piperidine-2-methanolHCID 2763853—
CatalystHCID 178419074HCID 178419074—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 2-formylpiperidine-1-carboxylateHCID 1065621970%

Reaction Steps

To a stirred solution of 2-hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester (0.737 g, 3.4 mmol) in dry CH2Cl2 (10 mL) was added 3 Å molecular sieves (1.03 g), N-methylmorpholine N-oxide (0.644 g, 5.5 mmol), and tetrapropylammonium perruthenate (72 mg, 0.21 mmol) and the mixture stirred at room temperature for 3 h. The reaction mixture was purified through a silica gel plug (Hexanes/EtOAc, 70:30 followed by 100:0) to afford the title aldehyde (0.500 g, 70%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07354934B2
Source datasetuspto-grants-2008_04
ORD IDord-ab822dd12a654e8784d1c79e4782a3b9
Source noteuspto-grants-2008_04