HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213528Generated: October 31, 2026
Toluene → Methyl 2-(4-(pyridin-2-yl)phenyl)acetate
https://huagongshe.com/reaction/2213528
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 2-(4-bromophenyl)acetate | HCID 316783 | — |
| Product | Methyl 2-(4-(pyridin-2-yl)phenyl)acetate | HCID 12094242 | — |
Reaction Steps
Under argon, 7.85 g (34.3 mmol) of methyl 4-bromophenylacetate are initially charged in 95 ml of toluene and, at room temperature, admixed with 7.97 g (61.7 mmol) of diisopropylethylamine, 9.50 g (37.7 mmol) of 2-trimethyl-stannylpyridine and 0.4 g (0.3 mmol) of tetrakis(triphenylphosphane)palladium(0). The mixture is then heated under reflux for 18 h. After cooling, the mixture is washed with in each case 100 ml of 1N hydrochloric acid and saturated sodium bicarbonate solution. The organic phase is discarded. The acidic and the basic aqueous phase are neutralized and in each case extracted with 100 ml of dichloromethane, and the combined organic phases are dried over sodium sulphate and freed from the solvent under reduced pressure. Example VII is obtained after silica gel chromatography (toluene/ethyl acetate gradient 5:1-1:1) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105553B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-c3e382950c7c43939931d5780fa12487 |
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| Source note | uspto-grants-2006_09 |
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