HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357480Generated: October 30, 2026
Sodium p-toluenesulfinate → 4,6-Dimethoxy-2-(4-toluenesulfonyl)pyrimidine
https://huagongshe.com/reaction/357480
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium p-toluenesulfinate | HCID 2723791 | — |
| Reactant | 2-Chloro-4,6-dimethoxypyrimidine | HCID 5152323 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4,6-Dimethoxy-2-(4-toluenesulfonyl)pyrimidine | HCID 15526620 | — |
Reaction Steps
4.38 g (25.0 mmol) of 2-chloro-4,6-dimethoxy-pyrimidine and 4.68 g (26.3 mmol) of sodium p-toluenesulfinate were heated in 25 ml of N,N-dimethylformamide to 100° C. while stirring. After 5 hours, the solvent was removed in a rotary evaporator at 60° C./20 mbar. The residue was taken up in 90 ml of water and 90 ml of ethyl acetate. After the organic phase had been separated off, the aqueous phase was again extracted with 75 ml of ethyl acetate. The combined organic phases was washed with water, dried over magnesium sulfate and evaporated. The residue was purified by chromatography on a silica gel column (eluent hexane/ethyl acetate 4:1). The title product was obtained from the product fraction in the form of a white powder in a yield of 3.79 g (15 percent of theory). The melting point of the title compound was 129.2° to 133.4° C. Other data concerning the title compound was:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840892 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-ad34ed859c19494e8c3a12b41718e85d |
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| Source note | uspto-grants-1998_11 |
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