HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863530Generated: October 29, 2026
Quinoline → rac. Z-1-benzyloxy-2-methyl-5-hepten-4-ol
https://huagongshe.com/reaction/1863530
Participants
| Role | Name | HCID | Charge |
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| Reactant | Quinoline | HCID 7047 | — |
| Reactant | Rac. 1-benzyloxy-2-methyhept-5-yn-4-ol | HCID 12923299 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Lindlars catalyst | HCID 131709914 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | rac. Z-1-benzyloxy-2-methyl-5-hepten-4-ol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04169209 |
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| Source dataset | uspto-grants-1979_09 |
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| ORD ID | ord-7ae5bd716896432c86d30cdd77fd1e7a |
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| Source note | uspto-grants-1979_09 |
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