Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 3-[(Pyrimidin-2-yl)oxy]propane-1,2-diol | HCID 20483411 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20483471 | HCID 20483471 | — |
Reaction Steps
13.6 g of p-toluenesulphonyl chloride are introduced over the course of 15 minutes, whilst stirring, into a solution of 11.8 g of 2-(2',3'-dihydroxy-propoxy)pyrimidine in 18 ml of pyridine which is cooled to -10° C. The reaction mixture is kept at 0° C. for 15 hours. Ice is then added followed by 20 ml of 6 N hydrochloric acid introduced whilst stirring. The mixture is then twice extracted with 150 ml of methylene chloride at a time. The extracts are washed with sodium bicarbonate solution, dried over sodium sulphate and evaporated. 2-(3'-p-Toluenesulphonyloxy-2'-hydroxy-propoxy)-pyrimidine is obtained as a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04195090 |
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| Source dataset | uspto-grants-1980_03 |
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| ORD ID | ord-771645554d36460cb43dbf0faa592f4d |
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| Source note | uspto-grants-1980_03 |
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