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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728277Generated: November 2, 2026

2-[4-(3-Acetoxy-1-butenyl)phenyl]-5-trimethylsilyloxy-pyridine → 2-[4-(3-Acetoxy-1-butyl)phenyl]-5-trimethylsilyloxy-pyridine

https://huagongshe.com/reaction/1728277

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[4-(3-Acetoxy-1-butenyl)phenyl]-5-trimethylsilyloxy-pyridineHCID 54198349—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product2-[4-(3-Acetoxy-1-butyl)phenyl]-5-trimethylsilyloxy-pyridineHCID 1901725185.2%

Reaction Steps

14 g of 2-[4-(3-acetoxy-1-butenyl)phenyl]-5-trimethylsilyloxy-pyridine, 2 g of palladium on active charcaol (10 wt. %) and 200 ml of tetrahydrofuran are hydrogenated in an analogous manner to Example 1(a) to give 12 g of 2-[4-(3-acetoxy-1-butyl)phenyl]-5-trimethylsilyloxy-pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05326497
Source datasetuspto-grants-1994_07
ORD IDord-56b38fed244c4848b6b315f28d65a503
Source noteuspto-grants-1994_07