HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911060Generated: October 25, 2026
Lithium Hexamethyldisilazide → 4-(benzyloxy)pyridin-2-amine
https://huagongshe.com/reaction/911060
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | 4-(Benzyloxy)-2-chloropyridine | HCID 53404197 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(benzyloxy)pyridin-2-amine | HCID 520084 | 70.2% |
Reaction Steps
4-(benzyloxy)-2-chloropyridine (18.6 g, 84.7 mmol), XPHOS (4.04 g, 8.47 mmol), and Pd2dba3 (3.88 g, 4.23 mmol) were mixed in THF (250 mL). LHMDS (93.1 ml, 93.1 mmol) was added and the reaction was heated at 50° C. for 1.5 hours. The solution was cooled and diluted with 1N HCl (50 mL) and stirred at ambient temperature for 2 hours. The reaction was concentrated and the residue was extracted with EtOAc. The aqueous layer was basified with saturated K2CO3 and the aqueous layer was extracted with EtOAc. The combined organic layers were dried and concentrated to give the desired product (11.9 g, 70.2% yield) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022222B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-fa84e86061a148fe8272fc9c06874a48 |
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| Source note | uspto-grants-2011_09 |
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