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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916661Generated: November 2, 2026

Potassium Hydroxide → 3-bromo-6,7,8,9-tetrahydro-5H-10-thia-7-aza-benzo[a]azulene

https://huagongshe.com/reaction/1916661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 3-bromo-5,6,8,9-tetrahydro-10-thia-7-aza-benzo[a]azulen-7-carboxylateHCID 69079455—
SolventEthanolHCID 702—
Product3-bromo-6,7,8,9-tetrahydro-5H-10-thia-7-aza-benzo[a]azuleneHCID 67364287—

Reaction Steps

30.0 g (53.5 mmol) KOH in 700 mL EtOH are added to a solution of 19.0 g (53.5 mmol) ethyl 3-bromo-5,6,8,9-tetrahydro-10-thia-7-aza-benzo[a]azulen-7-carboxylate. EtOH is distilled off at normal pressure and the residue is taken up in water. The solution is acidified with HCl. Then it is made basic with NaOH and the aqueous phase is extracted four times with chloroform. The organic phase is dried over Na2SO4 and K2CO3 and the solvent is eliminated i.vac. The purification is carried out by repeated column chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618132B2
Source datasetuspto-grants-2013_12
ORD IDord-9c1ca038d9754db294e1a90cb777c17b
Source noteuspto-grants-2013_12