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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628237Generated: October 29, 2026

Dithiooxamide → HCID 86706807, compound

https://huagongshe.com/reaction/628237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDithiooxamideHCID 2777982—
ReactantHCID 86706806HCID 86706806—
ProductHCID 86706807HCID 8670680729%

Reaction Conditions

Temperature200 °C

Reaction Steps

Under a nitrogen atmosphere, 2-formyl-3-(2-butyloctoxy)thiophene (7 g, 23.6 mmol) and rubeanic acid (1.42 g, 11.8 mmol) were added to a flask equipped with Dean-Stark, then heated to 200° C., and stirred for five hours. Then, the reaction mixture was extracted with chloroform, and an organic layer was washed with a saturated saline solution and water. The organic layer was dried with anhydrous magnesium sulfate, and, after filtration, the solvent was distilled off under reduced pressure. By separating and purifying the obtained reaction mixture by silica gel column chromatography in which a mixed solvent of hexane and chloroform was used as a mobile phase, a target substance was obtained as a yellow solid (29% yield). 1H-NMR (400 MHZ, CDCl3, TMS) δ 7.31 (d, J=5.6 Hz, 1 H), 6.88 (d, J=5.6 Hz, 1 H), 4.13 (d, J=4.8 Hz, 2 H), 1.25 (m, 17 H), 0.88 (m, 6 H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09312491B2
Source datasetuspto-grants-2016_04
ORD IDord-562fc6b5a0f74101a7970423a33d01e4
Source noteuspto-grants-2016_04