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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604274Generated: October 31, 2026

2-Aminothiophenol → 2-Methyl-2,3-dihydro-1H-phenothiazin-4(10H)-one

https://huagongshe.com/reaction/1604274

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantHCID 19602601HCID 19602601—
SolventDimethyl SulfoxideHCID 679—
Product2-Methyl-2,3-dihydro-1H-phenothiazin-4(10H)-oneHCID 15621528—

Reaction Steps

A mixture of ter butyl 6-methyl-2,4-dioxocyclohexane-1-carboxylate, 7c (3.09 g, 13.7 mmole) and 2-aminothiophenol, 6 (X=H, 1.71 g, 13.7 mmole) in DMSO (10 mL) is placed in a preheated heating mantle. The reaction mixture is stirred and refluxed for 0.5 h. Upon cooling, the reaction mixture forms a solid. The crystals are filtered and the remaining mother liquid is poured into cold water, whereupon further precipitation occurs. Each precipitate was separately recrystallized twice from MeOH and proves to be identical. An analytical sample of 4d, (R=H), mp 278° C. occurs as light orange crystals; yield: 0.46 g (15.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994349
Source datasetuspto-grants-1999_11
ORD IDord-c53f69dc79354be285c8875f7892502c
Source noteuspto-grants-1999_11