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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702186Generated: October 30, 2026

1,3-Cyclohexanedione, 2-bromo-5,5-dimethyl- → HCID 3123575, compound

https://huagongshe.com/reaction/1702186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Cyclohexanedione, 2-bromo-5,5-dimethyl-HCID 70958—
ReactantSodium AcetateHCID 517045—
ReactantMethylthioureaHCID 2723704—
SolventAcetic AcidHCID 176—
ProductHCID 3123575HCID 312357581.3%

Reaction Steps

82 g of 2-bromo-5,5-dimethylcyclohexane-1,3-dione, 40 g of sodium acetate and 50 g of N-methylthiourea are dissolved in 500 ml of acetic acid. The mixture is stirred at room temperature until the weakly exothermic reaction has subsided, and then refluxed for 3 hours. The reaction mixture is then concentrated to one third of its volume in a rotary evaporator, poured into 100 ml of water and cooled to 0° C. The precipitate is collected by filtration and dried in vacuo at 80° C., affording 64 g of 2-methylamino-5,5-dimethyl-7-oxo-4,5-dihydro-6H-benzthiazole with a melting point of 217°-218° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380640
Source datasetuspto-grants-1983_04
ORD IDord-aa00dd27246240d9a70a7ba0ce1cd3d7
Source noteuspto-grants-1983_04