HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665981Generated: October 31, 2026
Hydrochloric Acid → 7-(Benzyloxy)-4-methyl-1,2-dihydronaphthalene
https://huagongshe.com/reaction/1665981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 6-(benzyloxy)-3,4-dihydronaphthalen-1(2H)-one | HCID 10682241 | — |
| Solvent | HCID 178418573 | HCID 178418573 | — |
| Product | 7-(Benzyloxy)-4-methyl-1,2-dihydronaphthalene | HCID 23121671 | — |
Reaction Steps
To a solution of the obtained 6-(benzyloxy)-3,4-dihydronaphthalen-1(2H)-one (34.5 g) in tetrahydrofuran (300 mL), methyl magnesium bromide (3M diethyl ether solution, 55 mL) was added at 0° C., followed by stirring at room temperature for 1 hour. The reaction mixture was cooled to 0° C. and poured into ice-saturated aqueous ammonium chloride solution. After adding 2N hydrochloric acid, the mixture was stirred at room temperature for 3 hours. Then, the resultant was extracted with ethyl acetate and the organic layer was successively washed with water and brine, dried and concentrated. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1) to thereby give the title compound (24.8 g) having the following physical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039674B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-9589c278b3694793928761f5b0f99650 |
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| Source note | uspto-grants-2011_10 |
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