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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461285Generated: November 1, 2026

Hexane → HCID 14835954, compound

https://huagongshe.com/reaction/1461285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantChloroselenobenzeneHCID 21928—
Reactant3-Methyl-5,6,7,8-tetrahydroquinolineHCID 120028—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14835954HCID 1483595498.6%

Reaction Steps

A solution of 5,6,7,8-tetrahydro 3 methylquinoline (7.5 g, 51 mmol) in tetrahydrofuran (100 ml) was treated under an atmosphere of nitrogen with 1.5M-butyllithium in hexane (35 ml, 52 mmol) at 0°. The resulting red solution was added to a solution of phenylselenyl chloride (10 g, 52 mmol) in tetrahydrofuran (50 ml) at 0°. After 30 min, water (100 ml) was added and the mixture concentrated in vacuo. The aqueous residue was partitioned between saturated aqueous sodium chloride (100 ml) and ether (100 ml). The organic phase was dried (Na2SO4) and evaporated in vacuo to give the crude product (15.2 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075303
Source datasetuspto-grants-1991_12
ORD IDord-c4236ae4f3ae4394a84935f10227ef7a
Source noteuspto-grants-1991_12