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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421491Generated: November 2, 2026

Acetic Anhydride → HCID 67214036, compound

https://huagongshe.com/reaction/2421491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 67213498HCID 67213498—
SolventPyridineHCID 1049—
ProductHCID 67214036HCID 6721403649%

Reaction Conditions

Temperature10 °C

Reaction Steps

The 3,7-dimethylamino-10H-phenothiazine obtained in Synthesis 7 was placed in a 250 cm3 round bottom flask and acetic anhydride ((H3CCO)2O, 40 cm3) and pyridine (10 cm3) were added, and the resulting solution was heated at 10° C. for 18 hours with stirring. The reaction mixture was cooled to room temperature and then poured carefully into ice-water while stirring to give a light brown solid, which was filtered using a standard Buchner funnel apparatus with a water aspirator, washed once with water (100 cm3), and dried in an oven at 60° C. for 3 hours to yield the title compound, which was recrystallised from ethanol by dissolving it in hot ethanol (100 cm3), adding activated charcoal (1 g), filtering to remove the charcoal, cooling the solution to 5° C. using an ice-water bath so that a precipitate formed (colourless crystals), and filtering using a standard Buchner filter with a water aspirator in order to collect the crystals. The crystals where then dried in an oven at 60° C. for 3 hours (MW 327.45, 4.25 g, 13.0 mmol, yield 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956183B2
Source datasetuspto-grants-2011_06
ORD IDord-1133deb989e24e8d9c90a4290714386d
Source noteuspto-grants-2011_06