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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186997Generated: November 1, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → (2-Chloro-4-cyano-5-methoxyphenyl)ethylene

https://huagongshe.com/reaction/1186997

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-(2-Chloro-4-cyano-5-methoxyphenyl)ethyl methanesulfonateHCID 86647306—
SolventCitric AcidHCID 311—
SolventDichloromethaneHCID 6344—
Product(2-Chloro-4-cyano-5-methoxyphenyl)ethyleneHCID 66643919—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2-(2-chloro-4-cyano-5-methoxyphenyl)ethyl methanesulfonate (274 mg, 0.945 mmol) in DCM (4 mL) was treated with DBU (0.712 mL, 4.73 mmol) and stirred for 3 hours at 50° C., then at RT for 12 hours. TLC (50% ethyl acetate/hexanes) showed complete conversion to a faster intense UV band for the product. The reaction was then diluted with DCM and aq. citric acid and the mixture was extracted twice with DCM. The organic layers were washed with brine, dried over sodium sulfate and concentrated in vacuo. Purification of the residue by flash chromatography (10-20% ethyl acetate/hexanes) afforded the title intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673920B2
Source datasetuspto-grants-2014_03
ORD IDord-c2eec8124cac451fb9c9a068fdad63f2
Source noteuspto-grants-2014_03