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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260613Generated: October 28, 2026

Allyl chloride → HCID 53906958, compound

https://huagongshe.com/reaction/2260613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 53833969HCID 53833969—
ProductHCID 53906958HCID 5390695886%

Reaction Steps

Using an analogous procedure to that described in Example 18, (2S,4R)-4-(tert-butyldimethylsilyloxy)-2-methyl-4-[3-(2-oxo-1,2,3,4-tetrahydroquinolin-6-ylthio)phenyl]tetrahydropyran was reacted with allyl chloride and the resultant product was treated with tetrabutylammonium fluoride to give (2S,4R)-4-[3-(1-allyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-ylthio)phenyl]-4-hydroxy-2-methyltetrahydropyran in 86% yield, m.p. 107°-109° C. (recrystallised from diethyl ether);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478842
Source datasetuspto-grants-1995_12
ORD IDord-30a45755a97548758920ebef63db6fd5
Source noteuspto-grants-1995_12