Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 3-Bromopropane-1-sulfonyl chloride | HCID 289329 | — |
| Reactant | Dimethyl (2-hydroxyethyl)phosphonate | HCID 2733833 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21396802 | HCID 21396802 | — |
Reaction Steps
3.9 g of dimethyl 2-hydroxyethylphosphonate and 5.9 g of pyridine were dissolved in 40 ml. of dry diethyl ether, and the solution was cooled with ice to -5° C. A solution of 6.0 g of γ-bromopropylsulfonyl chloride in 30 ml. of dry diethyl ether was added dropwise to the cooled solution by means of a dropping funnel. After the addition, the mixed solution was allowed to stand for 24 hours at 0° to 5° C. The reaction mixture was poured into 50 ml. of 5% hydrochloric acid, and extracted with diethyl ether. The extract was dried over anhydrous sodium sulfate, and the solvent was distilled off at reduced pressure. The product was further dried at room temperature at 0.7 mmHg for 18 hours to afford dimethyl 2-(3-bromopropylsulfonyloxy)ethylphosphonate as a colorless oil in a yield of 75 mol %. The product showed the following characteristic values.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04059431 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-05d4a1a755924239adc6cd3119a02918 |
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| Source note | uspto-grants-1977_11 |
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