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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212146Generated: November 1, 2026

Tetrahydrofuran → HCID 10142972, compound

https://huagongshe.com/reaction/2212146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 21964303HCID 21964303—
ProductHCID 10142972HCID 10142972—

Reaction Steps

Oxalyl chloride (1.05 mL) was added dropwise to a stirring solution of {1-(4-methylbenzyl)-5-[4-(trifluoromethoxy)phenyl]-1H-indol-2-yl}methyl acetate (0.515 g) in THF (17 mL) at room temperature over a period of 5 minutes under a nitrogen atmosphere. After the reaction mixture was stirred at room temperature for 4 hours, the reaction was quenched carefully with water. The aqueous mixture was extracted with ethyl acetate. The extract was washed with water, and brine, dried over anhydrous magnesium sulfate, and concentrated to give the title compound as a light brown solid, mp: 79–80° C. Mass spectrum (ESI, [M−H]−) m/z 524. 1HNMR (400 MHz, DMSO-d6): δ 14.50 (br s, 1H), 8.20 (s, 1H), 7.74 (d, 2H, J=8.55 Hz), 7.70 (d, 1H, J=8.69 Hz), 7.62 (d, 1H, J=8.55 Hz), 7.47 (d, 2H, J=8.25 Hz), 7.15 (d, 2H, J=7.88 Hz), 6.99 (d, 2H, J=7.78 Hz), 5.64 (s, 2H), 5.53 (s, 2H), 2.25 (s, 3H), and 1.83 ppm (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101903B2
Source datasetuspto-grants-2006_09
ORD IDord-f19920501f054c54a1e667bed68e267c
Source noteuspto-grants-2006_09