HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626885Generated: October 26, 2026
Hydrogen iodide → HCID 90014635, compound
https://huagongshe.com/reaction/626885
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | 2-Chloro-4-methyl-6-(4-trifluoromethyl-phenyl)-pyrimidine | HCID 57468614 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90014635 | HCID 90014635 | 85.8% |
Reaction Steps
Hydroiodic acid (57% in water, 9.68 mL, 73.41 mmol) was added portionwise to 2-chloro-4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine (which may be prepared as described in Description 11) (1.38 g, 5.06 mmol) in DCM (30 mL) at 20° C. and the dark mixture was stirred for 18 hrs. The mixture was quenched by the addition of sat. aq. K2CO3 (care: gas evolved). After basification, satd. aq. sodium metabisulphite was added and stirring was continued for 5 mins. The mixture was diluted with further DCM and the phases were separated. The organic layer was dried (Na2SO4) and the solvent evaporated to afford 2-iodo-4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine (D12) (1.58 g, 4.34 mmol, 85.7% yield) a yellow solid, containing about 20% of the reduced H-compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309254B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-ae0078101b7e4cf59f239ea49d0a01d6 |
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| Source note | uspto-grants-2016_04 |
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