HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992182Generated: October 29, 2026
Hydrochloric Acid → 2-Methoxy-6-propylnaphthalene
https://huagongshe.com/reaction/992182
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | 2-Bromo-6-methoxynaphthalene | HCID 78786 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | [1,2-Bis(diphenylphosphino)ethane]dichloronickel(II) | HCID 2734542 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methoxy-6-propylnaphthalene | HCID 3023663 | 101.8% |
Reaction Steps
To a solution of 200 g of 2-bromo-6-methoxynaphthalene and 2.5 g of dichloro[1,2-bis(diphenylphosphino)ethane]nickel (II) in 200 ml of tetrahydrofuran (THF) was added dropwise a Grignard reagent prepared from 125 g of propyl bromide and 27 g of magnesium under nitrogen atomsphere. The reaction mixture was further stirred for 1 hour, and then poured into water. To the reaction mixture was then added diluted hydrochloric acid. The resulting organic phase was then separated. The resulting aqueous phase was extracted with toluene. The organic phase and the material thus extracted were together washed sequentially with water, saturated aqueous solution of sodium bicarbonate, water and saturated brine, and then dehydrated and dried over anhydrous sodium sulfate. The solvent was then distilled off to obtain 172 g of 2-methoxy-6-propylnaphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06468607B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-98420df65afb4476ac6d8818898a423d |
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| Source note | uspto-grants-2002_10 |
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