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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168314Generated: October 31, 2026

Potassium tert-butoxide → HCID 58197246, compound

https://huagongshe.com/reaction/2168314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 58197149HCID 58197149—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58197246HCID 5819724641.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 4-(5-bromo-2-fluorobenzoyl)-4-hydroxycyclohexanone (1.0055 g, 3.19 mmol, 1.0 equiv) in THF (30 mL) was added 95% t-BuOK (0.3440 g, 2.91 mmol, 0.9 equiv) portionwise. The resulting mixture was heated at 100° C. for 1 h. The reaction mixture was then cooled with an ice bath and quenched with H2O, extracted with ethyl acetate, dried over Na2SO4. After the solvents were evaporated, the residue was purified by chromatography on silica gel eluted with hexanes/ethyl acetate to afford 0.3889 g (41%) of 5-bromo-3H-spiro[benzofuran-2,1′-cyclohexane]-3,4′-dione as a white solid. LC-MS tR=1.58 min in 3 min chromatography, m/z 295, 297 (MH+); 1H NMR (400 MHz, CDCl3) δ 7.82-7.81 (m, 1H), 7.76-7.73 (m, 1H), 7.10-7.07 (m, 1H), 2.81-2.72 (m, 2H), 2.60-2.55 (m, 2H), 2.29-2.21 (m, 2H), 2.08-2.03 (m, 2H); 13C NMR (100 MHz, CDCl3) δ 208.25, 200.80, 169.71, 140.99, 127.47, 121.58, 115.55, 114.81, 88.10, 36.68, 31.86.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045500B2
Source datasetuspto-grants-2015_06
ORD IDord-5979f7962bf74c079407aa38d83d2e7c
Source noteuspto-grants-2015_06