HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085028Generated: October 26, 2026
Dihydrocoumarin → 2-(3-Hydroxy-3-methylbutyl)phenol
https://huagongshe.com/reaction/1085028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dihydrocoumarin | HCID 660 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Product | 2-(3-Hydroxy-3-methylbutyl)phenol | HCID 2778953 | — |
Reaction Steps
To an ice-cooled solution of methyl magnesium bromide in ether (104 ml × 2.7M; 0.28 mole) was added slowly, under nitrogen, a solution of 13.8 g (0.093 mole) of dihydrocoumarin (Compound 28, Scheme 8) in 230 ml of dry ether. The cooling bath was then removed and the mixture stirred for a further 16 hours. The reaction mixture was then poured onto 300 g of ice and 10 ml of conc. H2SO4 and the mixture was stirred to ensure dissolution. The organic layer was then separated and the aqueous layer was extracted with 2×100 ml of ether. The organic layers were combined and washed successively with 70 ml portions of water, saturated NaHCO3, 2M Na2S2O3 and saturated NaCl and then dried (Na2SO4). The solution was then filtered and the filtrate concentrated in-vacuo to give the title compound as a white solid. PMR (CDCl3) : & 1.30 (6H, s), 1.80 (2H, t, J~7.5 Hz), 2.12 (1H, broad s), 2.73 (2H, t, J~7.5 Hz), 6.80-6.87 (2H, m), 7.00 (1H, broad s), 7.07-7.14 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05006550 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-d389777cb76147ad962fe01d03940a12 |
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| Source note | uspto-grants-1991_04 |
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