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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3669생성일: 2026년 10월 23일

P-Toluic Acid → 2,5-Pyrrolidinedione, 1-[(4-methylbenzoyl)oxy]-

https://huagongshe.com/ko/reaction/3669

반응식

참여 물질

역할이름HCID투입량
반응물P-Toluic AcidHCID 7470—
반응물TriethylamineHCID 8471—
반응물Diphenyl chlorophosphateHCID 75654—
반응물N-HydroxysuccinimideHCID 80170—
용매Ethyl AcetateHCID 8857—
용매tert-Butyl methyl etherHCID 15413—
생성물2,5-Pyrrolidinedione, 1-[(4-methylbenzoyl)oxy]-HCID 642240494%

반응 단계

2.42 g (0.021 mol) of N-hydroxysuccinimide and 5.06 g (0.050 mol) of triethylamine were initially introduced into 5 ml of ethyl acetate and the suspension was stirred at room temperature. 2.72 g (0.020 mol) of solid 4-toluic acid were added to this suspension in the course of 5 min. and then a solution of 5.64 g (0.21 mol) of diphenyl chlorophosphate was added dropwise in the course of 20 min., the reaction mixture warming to about 35° C. The mixture was stirred at room temperature for 1 hour until the reaction was complete. The reaction mixture was then diluted with 100 ml of ethyl acetate and the organic phase was washed with 50 ml each of water, 2N hydrochloric acid and 10% strength aqueous sodium hydrogencarbonate solution and then evaporated. 4.65 g of crude product were isolated, which was then stirred at room temperature for 30 minutes with 20 ml of methyl tert-butyl ether. The white crystalline solid was filtered off and dried at 50° C. and 10 mbar. 4.28 g (94%) of 4-toluic acid succinimidyl ester were isolated.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05734064
출처 데이터셋uspto-grants-1998_03
ORD IDord-fa9e36ab9df044eca0ae8f17c3acb777
출처 메모uspto-grants-1998_03