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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376967Generated: October 25, 2026

Pentane → 5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuran

https://huagongshe.com/reaction/1376967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
ReactantHeptyltriphenylphosphonium bromideHCID 2724567—
Reactant5-Benzyloxy-4-t-butyl-2-formylbenzofuranHCID 23442879—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuranHCID 5430872291.2%

Reaction Steps

A pentane solution (2.6 ml, 4.2 mmol) of 1.6M n-butyllithium was added dropwise to a solution of n-heptyltriphenylphosphonium bromide (1.84 g, 4.2 mmol) in tetrahydrofuran (10 ml) under a nitrogen atmosphere. After stirring the mixture at room temperature for 30 min, a solution of 5-benzyloxy-4-tert-butyl-2-formylbenzofuran (1.0 g, 3.2 mmol) in tetrahydrofuran (10 ml) was added dropwise. Subsequently, the mixture was stirred at room temperature for 30 min, poured into ice water and subjected to extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and water, then dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica Gel chromatography (chloroform) to afford 5-benzyloxy-4-tert-butyl-2-(1-octenyl)benzofuran [1.14 g (yield, 91%)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663373
Source datasetuspto-grants-1997_09
ORD IDord-8f9839940081438eb9ea5381c16840c8
Source noteuspto-grants-1997_09