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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464555Generated: October 30, 2026

Triethylamine → HCID 20262080, compound

https://huagongshe.com/reaction/464555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-DifluoronitrobenzeneHCID 67967—
ReactantMethallyl mercaptanHCID 11051576—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20262080HCID 2026208085.2%

Reaction Steps

To a solution of 5.0 g (0.031 mole) of 2,4-difluoronitrobenzene and 2.8 g (0.031 mole) of 2-methyl-2-propenethiol in 25 ml of tetrahydrofuran at room temperature was added dropwise 3.1 g (0.031 mole) of triethylamine. The reaction mixture was stirred at room temperature for forty-eight hours and then at 50° C. for eight hours. The tetrahydrofuran was removed under reduced pressure, and water was mixed with the residue. This aqueous mixture was extracted with chloroform. The chloroform extract was washed with water, dried, and the chloroform evaporated under reduced pressure, leaving an oily residue. Distillation of this residue under reduced pressure yielded 6.0 g of 2-(2-methyl-2-propenylthio)-4-fluoronitrobenzene. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04548640
Source datasetuspto-grants-1985_10
ORD IDord-b717fa2e502249e48bdfc2b1afd2558c
Source noteuspto-grants-1985_10