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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089866Generated: November 1, 2026

Toluene → HCID 19978531, compound

https://huagongshe.com/reaction/1089866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantIsopropanolHCID 3776—
ReactantMaleic AnhydrideHCID 7923—
ReactantPhenol, 4-[1-(4-aminophenyl)-1-methylethyl]-HCID 11148864—
CatalystSulfuric AcidHCID 1118—
SolventWaterHCID 962—
ProductHCID 19978531HCID 19978531478.3%

Reaction Steps

To a reaction vessel equipped with a stirrer, thermometer and an azeotropic distillation trap, 60 g (0.1 mole) of maleic anhydride, 480 g of toluene and 2.6 g of 95% sulfuric acid were charged and heated to a reflux temperature. A solution containing 114 g (0.5 mole) of 2-(4-hydroxyphenyl)-2-(4-aminophenyl)propane in 160 g of N,N'-dimethylacetamide was dropwise added from a dropping funnel over 4 to 5 hours and reacted for 5 hours at the same temperature. Generated water by the reaction was removed by azeotropic distillation. After completing the reaction, the reaction mixture was cooled to 80° to 90° C. and the solvent was successively removed under reduced pressure. The organic layer thus obtained was mixed with 100 ml of isopropyl alcohol and then 300 ml of water was added and stirred for 0.5 to 1 hour to precipitate crystals. The crystals were filtered and dried to obtain 147 g of 2-(4-hydroxyphenyl)-2-(4-maleimidophenyl)propane as yellow crystals. The yield was 96%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05079331
Source datasetuspto-grants-1992_01
ORD IDord-6b98322b84b140c8be2bd0c3e57d0e05
Source noteuspto-grants-1992_01