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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464500Generated: October 31, 2026

Quinoline → HCID 15230863, compound

https://huagongshe.com/reaction/1464500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinolineHCID 7047—
ReactantHCID 19088069HCID 19088069—
SolventEthyl AcetateHCID 8857—
ProductHCID 15230863HCID 1523086394%

Reaction Steps

Rindler catalyst (90 mg) and quinoline (15 μl) were added to a solution of 7-(3,5,6-trimethyl-1,4-benzoquinon -2-yl)-7-phenyl-2-heptyn-1-ol (1.01 g, 3.0 mmole) in ethyl acetate (20 ml), and catalytic reduction was carried out at room temperature. 3 Hours later, when absorption (73 ml) of hydrogen was almost stopped, the reaction was suspended and the catalyst was filtered out. The ethyl acetate was distilled off under reduced pressure, and the residue was chromatographed on a silica gel column to elute with isopropayl ether to give (Z)-7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenyl-2-hepten-1-ol (0.95 g, 94%). Its typical physical properties and nuclear magnetic resonance spectrum data are shown in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05304658
Source datasetuspto-grants-1994_04
ORD IDord-32150750856d4c69829a19404c37a64c
Source noteuspto-grants-1994_04