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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702185Generated: October 30, 2026

1,3-Cyclohexanedione, 2-bromo-5,5-dimethyl- → 2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-one

https://huagongshe.com/reaction/1702185

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Cyclohexanedione, 2-bromo-5,5-dimethyl-HCID 70958—
ReactantThioureaHCID 2723790—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventSodium BicarbonateHCID 516892—
Product2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-oneHCID 58787483.7%

Reaction Steps

28 g of 2-bromo-5,5-dimethylcyclohexane-1,3-dione and 11.7 g of thiourea are dissolved in 200 ml of ethanol. After the weakly exothermic reaction has subsided, the mixture is refluxed for a further 6 hours. The solution is diluted with 400 ml of water and neutralised with saturated sodium bicarbonate solution. The precipitated crystals are collected by filtration and dried in vacuo at 80° C., affording 21 g of 2-amino-5,5-dimethyl-7-oxo-4,5-dihydro-6H-benzthiazole with a melting point of 203°-205° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380640
Source datasetuspto-grants-1983_04
ORD IDord-1107443d59d84ce4ab9c5456efada9c3
Source noteuspto-grants-1983_04