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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179118Generated: November 2, 2026

HCID 85844986, compound → HCID 67211384, compound

https://huagongshe.com/reaction/1179118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 85844986HCID 85844986—
CatalystHCID 178511488HCID 178511488—
SolventSodium HydroxideHCID 14798—
ProductHCID 67211384HCID 6721138488.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.26 g (4.50 mmol) of N-(2,5-dimethoxyphenyl)cyclohexanecarbothioamide is dissolved in 100 ml of a 1.5 M sodium hydroxide solution (100 ml) and the reaction medium is cooled down to 0° C. before adding 25 ml of a freshly prepared 20% aqueous solution of potassium ferricyanide (5.05 g of K3[Fe(CN)6]; 3.4 eq.). The reaction mixture is maintained under stirring at ambient temperature for 24 hours, then 1.1 g (yield=88%) of the expected benzothiazole derivative is obtained by filtration, washing with cold water and drying under reduced pressure in the presence of P2O5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279467B2
Source datasetuspto-grants-2007_10
ORD IDord-a9028579f23b430fb54338361e6ad709
Source noteuspto-grants-2007_10