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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241690Generated: October 31, 2026

Dimethyl Sulfate → HCID 11300689, compound

https://huagongshe.com/reaction/1241690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantSodium hydrideHCID 24758—
Reactant2-(3-Bromoanilino)benzoic acidHCID 14952461—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
SolventDimethylformamideHCID 6228—
ProductHCID 11300689HCID 1130068926%

Reaction Conditions

Temperature100 °C

Reaction Steps

(Method E-1) 2-(3-Bromo-phenylamino)benzoic acid, 13 (9.5 g, 32.5 mmol) was dissolved in conc. sulphuric acid (50 ml) and heated to 100° C. for 40 mins. After cooling, water was added slowly giving a green solid. The solid was filtered off and washed with water, and dried over phosphorous pentoxide. The crude material was partially dissolved in DMF (100 ml) and slowly added under nitrogen to sodium hydride (3.75 g, 156 mmol) in DMF (50 ml), and the mixture stirred for 30 mins. Dimethyl sulphate (12 ml, 72 mmol) was added and stirring continued for a further 30 mins before adding acetic acid (1 ml), then water (400 ml). The precipitate was filtered off, and the crude mix of 1 and 3-bromo acridones separated by column chromatography to give the title compound (2.43 g, 8.86 mmol, 26% over 2 steps). See, for example, Hodgeman et al., 1972.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115619B2
Source datasetuspto-grants-2006_10
ORD IDord-95efac1897a9493aad165ca19f698252
Source noteuspto-grants-2006_10