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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482977Generated: October 30, 2026

3-Methyl-8-(trimethylsilyl)-5,6,7,8-tetrahydroquinoline → HCID 178506786, compound

https://huagongshe.com/reaction/482977

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-8-(trimethylsilyl)-5,6,7,8-tetrahydroquinolineHCID 20244518—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 178506786HCID 178506786—

Reaction Steps

A mixture of a solution of 1.5 molar n-butyl lithium in hexane (12.9 ml, 20 mM) and THF (10 ml), maintained at 5° was treated with a solution of 5,6,7,8-tetrahydro-8-trimethylsilyl-3-methylquinoline (4.34 g 20 mM) to obtain 5,6,7,8-tetrahydro-8-lithio-8- trimethylsilyl-3-methylquinoline. After 0.5 hour a solution of t-butyldimethylsilyl isothiocyanate (7.0 g 40 mM) was added and the mixture allowed to warm to 20° over 12 hours. The reaction was quenched with 2N hydrochloric acid and stirred 1 hour. The mixture was extracted with ether, the aqueous phase adjusted to pHlO and extracted with ether. The organic extracts were dried and evaporated to give the title compound (3 g, 85%) identical with authentic material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04577022
Source datasetuspto-grants-1986_03
ORD IDord-de8a38a423df440a8fba92f36d143f39
Source noteuspto-grants-1986_03