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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480507Generated: October 27, 2026

Acetic Anhydride → HCID 86699468, compound

https://huagongshe.com/reaction/1480507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 71692790HCID 71692790—
Reactant3-(5-Chloro-2,3,3-trimethyl-3H-pyrrolo[2,3-b]pyridin-7-ium-7-yl)propane-1-sulfonateHCID 86699466—
ReactantHCID 178419561HCID 178419561—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
ProductHCID 86699468HCID 86699468130.1%

Reaction Conditions

Temperature115 °C

Reaction Steps

A 100-mL round-bottom flask fitted with a reflux condenser was charged with 3-(5-chloro-2,3,3-trimethyl-3H-pyrrolo[2,3-b]pyridin-7-ium-7-yl)propane-1-sulfonate (55, 500 mg), sodium 2,3,3-trimethyl-1-(3-sulfonatopropyl)-3H-indolium-5-sulfonate (4, 500 mg), (E)-N—((Z)-2-bromo-3-(phenylamino)allylidene)benzenaminium bromide (8, 100 mg), pyridine (1 mL), and acetic anhydride (10 mL) were added to the flask. The mixture was heated at 115° C. for 2 h, allowed to cool to room temperature, and diluted with ethyl ether (25 mL). The resulting dark blue dye precipitate was collected by filtration, dissolved in water (20 mL), and purified by preparative reverse-phase HPLC to afford the 9 as a blue powder (285 mg, 50%, UV 668 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408924B2
Source datasetuspto-grants-2016_08
ORD IDord-428cdf4a8421424d8459f21d0a920e98
Source noteuspto-grants-2016_08