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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706905Generated: October 31, 2026

2-Bromo-5-nitrothiazole → HCID 20333091, compound

https://huagongshe.com/reaction/1706905

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-nitrothiazoleHCID 18211—
ReactantHCID 178510538HCID 178510538—
SolventMethanolHCID 887—
ProductHCID 20333091HCID 2033309179%

Reaction Steps

To a solution of 4.36 (0.02 mol.) of 3,5-di(sodiomercapto)-4-isothiazole carbonitrile in methanol was added 8.4 g (0.04 mol.) of 2-bromo-5-nitrothiazole. A yellow-brown solid begins to precipitate almost immediately. The reaction mixture is stirred for an additional 2 hours at room temperature (~22° C.). The precipitate is collected by suction filtration, washed with water and methanol and dried in vacuo to yield 6.77 g (79% yield from the isothiazole) of a tan solid, m.p. 197°-199.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04209522
Source datasetuspto-grants-1980_06
ORD IDord-81ee75c9b6064dae8e2192c767d5ce96
Source noteuspto-grants-1980_06