HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168616Generated: October 27, 2026
Hydrochloric Acid → 5-(1-Hydroxy-5-methoxypentyl)-2-norbornene
https://huagongshe.com/reaction/1168616
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Chloro-4-methoxybutane | HCID 87363 | — |
| Reactant | Bicyclo(2.2.1)hept-5-ene-2-carboxaldehyde | HCID 95117 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(1-Hydroxy-5-methoxypentyl)-2-norbornene | HCID 22679043 | 75.4% |
Reaction Steps
In 300 g of tetrahydrofuran was dissolved 122.6 g of 1-chloro-4-methoxybutane. The solution was added dropwise to 24.3 g of metallic magnesium over 2 hours and below 60° C. Agitation was continued for 2 hours at room temperature. To the solution, 122.2 g of 5-norbornene-2-carbaldehyde was added dropwise over one hour and below 50° C. Agitation was continued for one hour at room temperature to drive the reaction to completion. Then 300 g of water and 44 g of 20% HCl were added to the solution, which was agitated. Extraction with 500 g of hexane gave the organic layer, which was washed with water, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuum. The oily matter thus obtained was distilled in vacuum, obtaining 158.6 g of 5-(1-hydroxy-5-methoxypentyl)-2-norbornene. The yield was 75.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06624335B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-13c6f83bf0f74ca2aa476057f187cee0 |
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| Source note | uspto-grants-2003_09 |
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