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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464554Generated: October 31, 2026

Triethylamine → HCID 13556902, compound

https://huagongshe.com/reaction/464554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAllyl MercaptanHCID 13367—
Reactant2,4-DifluoronitrobenzeneHCID 67967—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13556902HCID 1355690263.5%

Reaction Steps

A solution of 2.3 g (0.031 mole) of allylthiol in 25 ml of tetrahydrofuran was added to 5.0 g (0.031 mole) of 2,4-difluoronitrobenzene in 25 ml of tetrahydrofuran at -30° C. To this mixture was added dropwise 3.1 g (0.031 mole) of triethylamine. The temperature was allowed to rise to room temperature and stirring was continued for four hours. The tetrahydrofuran was evaporated under reduced pressure, and water and diethyl ether were added to the residue. The ether layer was separated and dried over anhydrous potassium carbonate. The ether was evaporated under reduced pressure, leaving a liquid residue. This residue was distilled at 105° C./1.2 mm of Hg, yielding 4.2 g of 2-allylthio-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-7d52994e3a0c4223ab5ad34b2c4316af
Source noteuspto-grants-1985_10