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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419585Generated: November 2, 2026

Quinoline → rac. Z-1-benzyloxy-2-methyl-5-hepten-4-ol

https://huagongshe.com/reaction/2419585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinolineHCID 7047—
ReactantRac. 1-benzyloxy-2-methyhept-5-yn-4-olHCID 12923299—
ReactantHCID 178418361HCID 178418361—
CatalystLindlars catalystHCID 131709914—
SolventHexaneHCID 8058—
Productrac. Z-1-benzyloxy-2-methyl-5-hepten-4-olHCID 12923294—

Reaction Steps

A mixture of 1 g. (4.31 mmoles) of rac. 1-benzyloxy-2-methylhept-5-yn-4-ol, 0.1 g. of Lindlar catalyst, 0.04 ml. of quinoline and 30 ml. of hexane was stirred in an atmosphere of hydrogen, at room temperature, for 40 minutes during which time approximately one equivalent of hydrogen was taken up. The catalyst was filtered and washed with hexane then the combined filtrate and washes were concentrated in vacuo giving 1.05 g. of oily product. This material was chromatographed on 50 g. of silica gel. Elution with 2:1 parts by volume and 1:1 parts by volume hexane-ether afforded 0.844 g. of a pale yellow oil. Evaporative distillation gave rac. Z-1-benzyloxy-2-methyl-5-hepten-4-ol as a colorless oil, b.p. 113°-123° C. (bath temperature) (0.25 mm Hg.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04107183
Source datasetuspto-grants-1978_08
ORD IDord-20d1a4d4b3794353acd66d9c9180b124
Source noteuspto-grants-1978_08