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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Chloro-4-methoxybutaneHCID 87363—
ReactantBicyclo(2.2.1)hept-5-ene-2-carboxaldehydeHCID 95117—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-(1-Hydroxy-5-methoxypentyl)-2-norborneneHCID 2267904375.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06624335B2
Source datasetuspto-grants-2003_09
ORD IDord-13c6f83bf0f74ca2aa476057f187cee0
Source noteuspto-grants-2003_09