HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129476Generated: October 29, 2026
Water → 4,5-Dichloro-6-isopropylpyrimidine
https://huagongshe.com/reaction/129476
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 4,5-Dichloro-6-ethylpyrimidine | HCID 11137668 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,5-Dichloro-6-isopropylpyrimidine | HCID 19371731 | — |
Reaction Steps
N-butyl lithium (1.6 mol solution in hexane, 19.4 ml) is added dropwise at 0° C., under a nitrogen atmosphere, to a solution of diisopropylamine (4.4 ml) in tetrahydrofuran (100 ml), and the mixture is stirred for 20 minutes. The solution is cooled to -78° C. and then 5 g of 4,5-dichloro-6-ethylpyrimidine in solution in 10 ml of tetrahydrofuran are added dropwise. The mixture is stirred at -78° C. for one hour and then brought to room temperature over a period of 2 hours. After the addition of water (200 ml), the mixture is extracted with ethyl acetate and the organic phase is dried over sodium sulfate and concentrated. Chromatography on silica gel (eluant: ethyl acetate/hexane 1:10) yields 3.8 g (71% of the theoretical yield) of 4,5-dichloro-6-isopropylpyrimidine in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05468751 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-446fd09f7f8242c8a4184ea50130ff89 |
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| Source note | uspto-grants-1995_11 |
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