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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706845Generated: October 30, 2026

Triethylamine → 1-Boc-piperidine-3-carboxaldehyde

https://huagongshe.com/reaction/706845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2763851—
SolventDimethyl SulfoxideHCID 679—
Product1-Boc-piperidine-3-carboxaldehydeHCID 996444868.5%

Reaction Steps

1-BOC-3-hydroxymethylpiperidine (2.15 g, 10 mmol) and triethylamine (3.03 g, 30 mmol) were dissolved in 10 mL DMSO, 15 mL DMSO solution of SO3Py (4.77 g, 30 mmol) was added to the above mixture in dropwise and the result mixture was stirred at rt for 2 hrs. The mixture was poured into 100 mL ice-water, extracted with EtOAc (100 mL×3), organic layer was washed with brine, dried with Na2SO4, filtered, and the filtrate was evaporated in vacuo. The crude product was purified by chromatography on silica gel (PE/EtOAc 5:1) to give 1.46 g product as colorless oil (68.5%). 1H NMR (300 MHz, CDCl3) δ: 9.70 (1 H, s), 3.91-3.93 (1 H, m), 3.62-3.67 (1 H, m), 3.29-3.36 (1 H, m), 3.05-3.13 (1 H, m), 2.40-2.45 (1 H, m), 1.95-1.97 (1 H, m), 1.63-1.72 (1 H, m), 1.49-1.59 (1 H, m), 1.46 (9 H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174996B2
Source datasetuspto-grants-2015_11
ORD IDord-cc06f228185b4187bea3875f6c72871f
Source noteuspto-grants-2015_11