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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445083Generated: October 28, 2026

Triethylamine → 2-{1-(1-Ethyl-1H-tetrazol-5-yl)piperidin-4-yl}ethanol

https://huagongshe.com/reaction/445083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium AzideHCID 33557—
ReactantHCID 57850772HCID 57850772—
CatalystMercuric ChlorideHCID 24085—
SolventDimethylformamideHCID 6228—
Product2-{1-(1-Ethyl-1H-tetrazol-5-yl)piperidin-4-yl}ethanolHCID 6852047041%

Reaction Steps

To a mixture of N-Ethyl-4-(2-hydroxyethyl)piperidine-1-carbothioamide (200 mg, 0.93 mmol), HgCl2 (277 mg, 1.02 mmol), and NaN3 (181 mg, 2.78 mmol) in DMF (2.5 mL) was added NEt3 (388 μL, 2.78 mmol) at rt. After stirring for 10 h, the reaction mixture was filtered, and the filter cake was washed with CH2Cl2. The combined filtrates and washings were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo, and the residue was purified by SiO2 chromatograph (60% EtOAc/hexane) to afford the titled compound (85 mg, 41%): 1H NMR (CDCl3) δ 4.18 (q, J=7.2 Hz, 2H), 3.75 (td, J=6.8, 5.2 Hz, 2H), 3.51 (brd, J=12.4, 2H), 3.03 (td, J=12.4, 2.8 Hz, 2H), 1.84 (brd, J=14.4 Hz, 2H), 1.71 (m, 1H), 1.59 (q, J=6.8 Hz, 2H), 1.56 (t, J=7.2 Hz, 3H), 1.48-1.38 (m, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476285B2
Source datasetuspto-grants-2013_07
ORD IDord-89a6e4a4a5f64a78a32afc833c8fd1a2
Source noteuspto-grants-2013_07