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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399472Generated: October 30, 2026

2-Chloro-1-fluoro-4-nitrobenzene → 3-Chloro-4-(2-thiazolylthio)nitrobenzene

https://huagongshe.com/reaction/399472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-fluoro-4-nitrobenzeneHCID 67688—
ReactantHCID 178527881HCID 178527881—
Product3-Chloro-4-(2-thiazolylthio)nitrobenzeneHCID 1896760226%

Reaction Steps

Using an analogous procedure to that described in the first paragraph of the portion of Example 8 which is concerned with the preparation of starting materials, 3-chloro-4-fluoronitrobenzene was reacted with 2-thiazolethiol to give a precipitated solid which was partitioned between ethyl acetate and water. The organic phase was dried (MgSO4) and evaporated to give 2-chloro-4-nitrophenyl 2-thiazolyl sulphide in 26% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05821246
Source datasetuspto-grants-1998_10
ORD IDord-ef581cff486446fe8604b1eb80db8312
Source noteuspto-grants-1998_10