HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907063Generated: October 25, 2026
Sodium Hydroxide → 4-Hydroxymethyl-1,6-heptadiene
https://huagongshe.com/reaction/1907063
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Diallylacetic Acid Ethyl Ester | HCID 10877522 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Hydroxymethyl-1,6-heptadiene | HCID 14895210 | 92.8% |
Reaction Steps
To a stirred solution of 2-allylpent-4-enoic acid ethyl ester (prepared above, 14.5 g, 86.2 mmol) in diethyl ether (125 mL) was added lithium aluminum hydride (3.3 g, 87 mmol) in portions slowly over a 30 minute period to cause vigorous gas evolution. When addition of the lithium aluminum hydride was complete, the reaction mixture was stirred for one more hour a room temperature, then 3.5 mL of water were added very slowly. Then 7 mL of a 10 weight percent solution of sodium hydroxide in water were added, followed by the addition of 10 more mL of water. The precipitated white solid was removed from the colorless solution by filtration. Solvent was removed from the solution at reduced pressure to leave 10.1 g of 2-allylpent-4-en-1-ol as a colorless oil whose structure was confirmed by NMR analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08597784B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-efcdcb0fe50646c8a299ad2c51e7bc84 |
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| Source note | uspto-grants-2013_12 |
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