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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977597Generated: October 29, 2026

Hydrochloric Acid → 2-bromo-6-[(1E)-(3RS)-3-tert-butyldiphenylsilyloxy-1-undecenyl]-pyridine

https://huagongshe.com/reaction/977597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant2-bromo-6-[(1E)-(3RS)-3-hydroxy-1-undecenyl)-pyridineHCID 15661708—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-bromo-6-[(1E)-(3RS)-3-tert-butyldiphenylsilyloxy-1-undecenyl]-pyridineHCID 8836338279.4%

Reaction Steps

A solution of 4 g of 2-bromo-6-[(1E)-(3RS)-3-hydroxy-1undecenyl]-pyridine in 20 ml of dimethylformamide is mixed with 4.1 g of tert-butyldiphenylsilyl chloride and 2.1 g of imidazole and stirred for 15 hours at room temperature. The reaction mixture is poured into 100 ml of diethyl ether, shaken out twice with 20 ml of 1 n hydrochloric acid, 4 times with 20 ml of saturated common salt solution, dried on sodium sulfate and concentrated by evaporation. The residue is chromatographed on silica gel with hexane/0-5% ethyl acetate. 5.5 g of 2-bromo-6[(1E)-(3RS)-3-tert-butyldiphenylsilyloxy-1-undecenyl]-pyridine is obtained as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614634
Source datasetuspto-grants-1997_03
ORD IDord-3ad7a85e943b42968c60fb29204804db
Source noteuspto-grants-1997_03