HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592169Generated: October 31, 2026
4-(Tributylstannyl)pyridazine → Tert-butyl 2-(3-methyl-4-(pyridazin-4-yl)phenyl)acetate
https://huagongshe.com/reaction/592169
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Tributylstannyl)pyridazine | HCID 6409733 | — |
| Reactant | Tert-butyl 2-(4-bromo-3-methylphenyl)acetate | HCID 58447742 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 2-(3-methyl-4-(pyridazin-4-yl)phenyl)acetate | HCID 58447683 | — |
Reaction Steps
A mixture of tert-butyl 2-(4-bromo-3-methylphenyl)acetate (855 mg, 3.00 mmol), 4-(tributylstannyl)pyridazine (1162 mg, 3.15 mmol), Pd(PPh3)4 (173 mg, 0.15 mmol) and DMF (10 ml) was stirred under argon atmosphere at 118° C. overnight. After cooled to room temperature, the mixture was concentrated by evaporation of DMF, redissolved in ethyl acetate (50 ml) and washed with water (50 ml×2). After dried over Na2SO4 and concentrated by evaporation, the mixture was subjected to silica gel column chromatography with ethyl acetate/hexanes (1:1) as eluent to give tert-butyl 2-(3-methyl-4-(pyridazin-4-yl)phenyl)acetate 134-2 as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238646B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-ec2b376708e74971a7d81ead885f2860 |
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| Source note | uspto-grants-2016_01 |
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