HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330797Generated: October 30, 2026
Methanol → Methyl 3-(5-hydroxypyrimidin-2-yl)benzoate
https://huagongshe.com/reaction/330797
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-(5-Hydroxypyrimidin-2-yl)benzoic acid | HCID 59484936 | — |
| Product | Methyl 3-(5-hydroxypyrimidin-2-yl)benzoate | HCID 59438048 | — |
Reaction Steps
32.7 ml (445 mmol) of thionyl chloride are added to a suspension of 88.0 g (366 mmol) of 3-(5-hydroxypyrimidin-2-yl)benzoic acid in 1.4 l of methanol, and the mixture is heated at 80° C. for 2 hours. 20 ml (276 mmol) of thionyl chloride and, after 2 hours, a further 10 ml (138 mmol) of thionyl chloride are then added. After each addition, the reaction mixture is stirred at 80° C. for 2 hours. The reaction mixture is evaporated to a volume of about 300 ml in vacuo. The precipitate formed is filtered off and dried in vacuo: methyl 3-(5-hydroxypyrimidin-2-yl)benzoate as brownish crystals; m.p. 219-223°; ESI 231 (M+H); HPLC: Rt.=2.58 min (method A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877751B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-d70f119443a3478ba0f952980077f553 |
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| Source note | uspto-grants-2014_11 |
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