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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441549Generated: October 29, 2026

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

https://huagongshe.com/reaction/441549

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 numberUS04041058
Source datasetuspto-grants-1977_08
ORD IDord-3016375809a04bfd8ba4b6b99635e5b1
Source noteuspto-grants-1977_08