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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261398Generated: November 2, 2026

Ethyl Acetate → HCID 67235382, compound

https://huagongshe.com/reaction/1261398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium trimethylsilanolateHCID 23668039—
ReactantHCID 68313529HCID 68313529—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 67235382HCID 6723538278.6%

Reaction Conditions

Temperature30 °C

Reaction Steps

Potassium trimethyl silanolate (0.105 g, 0.82 mmol) was added to a solution of 1-(1-allylcyclopropylsulfonyl)-4,5-difluoro-3-(2-fluoro-4-iodophenyl)-1H-benzofuro[6,7-d]imidazol-2(3H)-one (0.230 g, 0.4108 mmol) in THF (5 mL) at 0° C. The reaction mass was stirred for 4 hours at 20-40° C. The reaction was monitored by TLC (10% ethyl acetate in hexane). The reaction mass was concentrated under reduced pressure and the concentrate was extracted with ethyl acetate. The organic layer was washed with water, brine solution, dried over sodium sulphate and concentrated under reduced pressure to afford the crude compound. Purification by column chromatography on silica gel (10% ethyl acetate in hexane) afforded 0.177 g of the product (78% yield). 1H NMR (CDCl3, 300 MHz): δ 7.54 (d, 1H), 7.40 (dd, 1H), 7.25 (s, 1H), 7.05 (bs, 1H), 6.99 (d, 1H), 6.32-6.39 (m, 1H), 6.22 (s, 1H), 5.65-5.75 (m, 1H), 5.19 (s, 1H), 5.10 (d, 1H), 2.88 (d, 2H), 1.15 (t, 2H), 0.75 (t, 2H). LCMS: 96.32%, m/z=548.8 (M+1). HPLC: 97.19%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470878B2
Source datasetuspto-grants-2013_06
ORD IDord-8792555b8a4747d78b262940cd25fc22
Source noteuspto-grants-2013_06