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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378280Generated: October 31, 2026

Hexane → HCID 69203973, compound

https://huagongshe.com/reaction/2378280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant3,5-DimethoxybenzaldehydeHCID 81747—
Reactant7-bromo-3,4-dihydro-2H-1,5-benzodioxepineHCID 2776394—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69203973HCID 6920397395%

Reaction Steps

To a solution of 7-bromo-3,4-dihydro-2H-benzo[b][1,4]dioxepine (1.7 g, 7.4 mmol) in THF (10 mL) was added a solution of n-butyllitium in hexane (2.6 mL, 2.5 N, 6.5 mmol) at −78° C. and kept for 20 min. To the mixture was added a solution of 3,5-dimethoxy-benzaldehyde (1.0 g, 6.0 mmol) in THF (10 mL) at −78° C. After 2 h, isopropanol (2 mL) and water (10 mL) was added to the mixture, and the cold bath was removed. The mixture was stirred at room temperature for 20 min. The mixture was extracted with ethyl acetate (50 mL) and water (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL). The combined organic layers was washed with HCl (1N, 50 mL), water (50 mL), brine (50 mL) and dried over MgSO4. Removal of solvent and chromatography (Silica Gel) gave (3,4-dihydro-2H-benzo[b][1,4]dioxepin-7-yl)-(3,5-dimethoxy-phenyl) -methanol as an oil (1.8 g, 95% yield): 1H NMR (CDCl3) δ 2.16-2.22 (m, 2H, CH2), 3.77 (s, 6H, 2CH3), 4.16-4.21 (m, 4H, 2CH2), 5.67 (d, J=3 Hz, 1H, CH), 6.35 (t, J=2 Hz, 1H, Ar), 6.54 (d, J=2 Hz, 1H, Ar), 6.92 (d, J=1 Hz, 2H, Ar), 6.98 (s, 1H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470723B2
Source datasetuspto-grants-2008_12
ORD IDord-848b6754f118489898ada89e610b9894
Source noteuspto-grants-2008_12