HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522177Generated: October 28, 2026
Potassium Chloride → HCID 90358076, compound
https://huagongshe.com/reaction/522177
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Chloride | HCID 4873 | — |
| Reactant | HCID 11753025 | HCID 11753025 | — |
| Reactant | Diacetyloxymercury | HCID 16683746 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 90358076 | HCID 90358076 | 72% |
Reaction Steps
To a suspension of Hg(OAc)2 (0.88 g, 2.8 mmol, 1.0 equiv) in dry THF (50 mL) under nitrogen atmosphere was added (2R,3R,4R,5R)-1,3,4,5-tetrakis(benzyloxy)hept-6-en-2-ol (1.5 g, 2.78 mmol, 1.0 equiv) dissolved in 20 mL of dry THF. The reaction was stirred at room temperature for 16 hours and then a saturated aqueous solution of potassium chloride (0.50 g, 4.5 mmol, 1.6 equiv) was added. After 30 minutes, the reaction mixture was diluted with EtOAc (80 mL), washed with water (20 mL), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The material thus obtained was purified by silica gel chromatography, eluting with 30% EtOAc in petroleum ether, to give (((2S,3S,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-yl)methyl)mercury(II) chloride as a pale yellow oil (1.5 g, 72%). 1H NMR (300 MHz, CDCl3) δ 7.45-7.15 (m, 20H), 4.62-4.39 (m, 7H), 4.33 (d, J=11.9 Hz, 1H), 4.24-4.11 (m, 1H), 4.08 (ddd, J=7.7, 5.9, 2.2 Hz, 1H), 3.89-3.76 (m, 2H), 3.72 (dd, J=4.2, 2.3 Hz, 1H), 3.68-3.57 (m, 1H), 3.39 (dd, J=8.5, 2.9 Hz, 1H), 2.18-1.96 (m, 2H). ESI (M+H2O) 792.0; calc for C35H37ClHgO5 774.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328134B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-8b079930b27b4eedbb743a16ccda4ce2 |
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| Source note | uspto-grants-2016_05 |
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