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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 57850772 | HCID 57850772 | — |
| Catalyst | Mercuric Chloride | HCID 24085 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-{1-(1-Ethyl-1H-tetrazol-5-yl)piperidin-4-yl}ethanol | HCID 68520470 | 41% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476285B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-89a6e4a4a5f64a78a32afc833c8fd1a2 |
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| Source note | uspto-grants-2013_07 |
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