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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651059Generated: November 2, 2026

Tetrahydrofuran → HCID 67793754, compound

https://huagongshe.com/reaction/1651059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
ReactantHCID 23051134HCID 23051134—
ProductHCID 67793754HCID 67793754—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-bromo-5-methylene-dibenzo[a,d]cycloheptene (5.7 g) in dry THF (20 ml), under an inert atmosphere, was added 9-borabicyclo[3,3,1]nonane (4.4 ml of a 0.5 molar solution in THF) at ambient temperature, and the reaction mixture was then refluxed for 3 h. After cooling in an ice bath the reaction was quenched by the slow addition of 2N sodium hydroxide solution (100 ml) and 30% hydrogen peroxide (20 ml). After stirring vigorously at 0° C. for 45 minutes the reaction mixture was allowed to warm to room temperature over a 2 h period then extracted with diethyl ether (3×200 ml). The combined organic layers were washed with brine (1×100 ml), dried (Na2SO4), filtered and concentrated in vacuo to leave a residue which was purified by chromatography on flash silica with 30% ethyl acetate in hexane as eluent to give the title compound (6.0 g) as a colourless oil. δ (360 MHz, CDCl3) 3.81 (2H, d, J=7.9 Hz, CH--CH2OH), 4.17 (1H, t, J=7.9 Hz, CH--CH2OH), 6.75 (1H, d, J=12 Hz, CHA =CHB), 6.89 (1H, d, J=12 Hz, CHA =CHB), 7.15-7.48 (7H, m, ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927819
Source datasetuspto-grants-1990_05
ORD IDord-6633ff0cc0fd4f358e7a4821ba490145
Source noteuspto-grants-1990_05