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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735977Generated: October 26, 2026

2-(4-(4-Hydroxy-1-butenyl)phenyl)-5-decyloxypyrimidine → 2-(4-(4-Hydroxybutyl)-phenyl)-5-decyloxypyrimidine

https://huagongshe.com/reaction/1735977

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(4-Hydroxy-1-butenyl)phenyl)-5-decyloxypyrimidineHCID 54459343—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product2-(4-(4-Hydroxybutyl)-phenyl)-5-decyloxypyrimidineHCID 1969490099%

Reaction Steps

0.38 g (1 mmol) of the thus obtained 2-(4-(4-hydroxy-1-butenyl)phenyl)-5-decyloxypyrimidine was dissolved in 20 ml of tetrahydrofuran, added with 0.05 g of 10% Pd/C and subjected to a hydrogenation reaction in a hydrogen atmosphere under normal pressure. The reaction was stopped when about 25 ml of hydrogen was consumed. Then 10% Pd/C was filtered out and the filtrate was concentrated to obtain 0.38 g of 2-(4-(4-hydroxybutyl)-phenyl)-5-decyloxypyrimidine (yield: 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05539115
Source datasetuspto-grants-1996_07
ORD IDord-5c67d8dada294132a8470df255669aff
Source noteuspto-grants-1996_07