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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394635Generated: October 28, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 17952717, compound

https://huagongshe.com/reaction/1394635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantThiophene-2,3-dicarbaldehydeHCID 573752—
ReactantHCID 10900225HCID 10900225—
SolventDichloromethaneHCID 6344—
ProductHCID 17952717HCID 1795271743%

Reaction Steps

A solution of 2,3-thiophenedicarboxaldehyde (600 mg, 4.28 mmol) in dichloromethane (50 ml) was cooled to 0° C. under an atmosphere of nitrogen. (1-Acetylamino-2-oxo-propyl)-phosphonic acid dimethyl ester (1.05 g, 4.70 mmol) was added [literature procedure: Kitamura, et al. Tet. Lett., 36(32), 1995, pp. 5769-5772], followed by DBU (0.471 ml, 4.70 mmol), and the mixture allowed to warm to ambient temperature overnight, then concentrated in vacuo, and the residue was then purified by flash chromatography (0-50% ethyl acetate in hexanes) to provide 1-thieno[2,3-c]pyridin-5-yl-ethanone as a white solid (326 mg, 43%). 1HNMR (250 MHz, CDCl3): δ 9.20 (s, 1H), 8.50 (d, 1H, J=1.02), 7.80 (d, 1H, J=5.36), 7.51 (d, 1H, J=5.36), 2.81 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348359B2
Source datasetuspto-grants-2008_03
ORD IDord-ecfad03223024fe8b8e611a8e1550ebe
Source noteuspto-grants-2008_03