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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271696Generated: October 31, 2026

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

https://huagongshe.com/reaction/271696

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 numberUS07452911B2
Source datasetuspto-grants-2008_11
ORD IDord-5d613efc1a91423484a71d7d78ac9e5d
Source noteuspto-grants-2008_11