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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639674Generated: November 2, 2026

Formic Acid → HCID 25191984, compound

https://huagongshe.com/reaction/1639674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantTetrahydrofuranHCID 8028—
Reactant2,1,3-Benzoxadiazole-5-carbonyl chlorideHCID 2735453—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 25191984HCID 25191984—

Reaction Steps

The preceding product (3.3 g) was dissolved in THF (50 ml) and methanol (50 ml), and freshly prepared Zn/Cu (15 g) was added followed by formic acid (5 ml). The mixture was stirred at room temperature for 20 minutes before filtering the solids and evaporating the solvent until ˜10 ml remained. Concentrated sodium hydroxide solution was added until pH 10 was reached and the mixture extracted with chloroform (100 ml) and the organic phase dried over sodium sulfate. Triethylamine (2 ml) was added followed by a solution of [2,1,3]-benzoxadiazole-5-carbonylchloride (0.5 g, 2.73 mmol) in chloroform (20 ml), slowly. After stirring the mixture for 20 minutes, water (100 ml) and H2SO4 (→pH2) were added and the aqueous phase extracted with chloroform (100 ml), dried over magnesium sulfate, and concentrated under vacuum to give an oil. The material was purified by silica gel chromatography eluting with hexane/ethyl acetate (3:2), to give after crystallization from dichloromethane/MTBE 133 mg of a white solid: mp=128-130° C., LC-MS, MH+=258; 1H NMR (300 MHz, CDCl3) δ 7.92 (s, 1H); 7.90 (d, 1H, J=6.3 Hz); 7.52 (d, 1H, J=6.3 Hz); 4.84 (s, 1H); 4.06 (s, 1H); 2.06-1.50 ppm (m, 10H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110584B2
Source datasetuspto-grants-2012_02
ORD IDord-0c34d1db452d4c3590b96e769974c7c7
Source noteuspto-grants-2012_02