HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530420Generated: October 27, 2026
Sodium Carbonate → 2-(2-chloro-4-pyrimidinyl)-6-methylPhenol
https://huagongshe.com/reaction/530420
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2,4-Dichloropyrimidine | HCID 77531 | — |
| Reactant | (2-Hydroxy-3-methylphenyl)boronic acid | HCID 18616946 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-chloro-4-pyrimidinyl)-6-methylPhenol | HCID 137131531 | — |
Reaction Steps
To a solution of 3.0 g (20 mmol) of 2,4-dichloro-pyrimidine in a 10:1 mixture of dioxane:water (220 mL) is added 3.3 g (22 mmol) of 2-hydroxy-3-methyl-phenyl boronic acid followed by 6.0 g (57 mmol) of sodium carbonate. Argon is bubbled through the solution for 15 min then 2.4 g (2.1 mmol) of tetrakis(triphenylphosphine)palladium (0) is added. The reaction is heated overnight at 100° C. then cooled to ambient temperature and filtered through diatomaceous earth. The filter pad is washed with EtOAc then placed on a new receiving flask and washed with a 1:1 mixture of MeOH:DCM. The filtrate is concentrated under reduced pressure to B-16 (1.60 g, 36.0%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353090B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-e719394409a34fa2bfe7bb57a1b3fcb8 |
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| Source note | uspto-grants-2016_05 |
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