HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397126Generated: October 27, 2026
Sodium Bicarbonate → S-Ethyl 3-(diethylphosphono)propionyloxymethyl carbonothioate
https://huagongshe.com/reaction/1397126
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(Diethylphosphono)propanoic acid | HCID 2773736 | — |
| Reactant | (Ethylsulfanyl)(iodomethoxy)methanone | HCID 11436522 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | S-Ethyl 3-(diethylphosphono)propionyloxymethyl carbonothioate | HCID 86666539 | 83% |
Reaction Steps
To a mixture of 3-(diethylphosphono)propanoic acid (79, 1.0 g, 4.76 mmol) in H2O (12 mL) and CH2Cl2 (12 mL) was added NaHCO3 (1.0 g, 11.9 mmol) and TBAHSO4 (1.62 g, 4.76 mmol). After stirring for 20 min, S-ethyl O-iodomethyl carbonothioate (1.17 g, 4.76 mmol) in CH2Cl2 (2 mL) was added. The biphasic reaction was stirred vigorously for 4 h 20 min and was diluted with water and CH2Cl2. The layers were separated, the organic layer was washed with H2O, 0.5 N HCl solution, saturated NaHCO3 solution, saturated NaCl solution, dried over MgSO4, filtered and concentrated to dryness. The crude product was triturated with Et2O and the solids were removed by filtration and rinsed with small portions of Et2O. After concentration, the combined filtrates were purified by flash chromatography on a Biotage™ flash chromatography system, using EtOAc as the eluent, to yield compound 80 (1.29 g, 83%) as a colorless oil: 1H NMR (400 MHz, CDCl3) δ 1.30-1.65 (m, 9H), 2.03-2.12 (m, 2H), 2.64-2.71 (m, 2H), 2.90 (q, J=7.4 Hz, 2H), 4.06-4.14 (m, 4H), 5.82 (s, 2H). 31P NMR (162 MHz, CDCl3) δ 30.45 (s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901072B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-d40f576338f0445b98665f0d7e9971fd |
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| Source note | uspto-grants-2014_12 |
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