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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 434532생성일: 2026년 10월 25일

Benzene → Carboxymethyl Benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-thiocarboxylate

https://huagongshe.com/reaction/434532

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물Thioglycolic AcidHCID 1133—
반응물KetorolacHCID 3826—
반응물DimethylformamideHCID 6228—
반응물Thionyl ChlorideHCID 24386—
용매Diethyl EtherHCID 3283—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물Carboxymethyl Benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-thiocarboxylateHCID 53956230—

반응 단계

To a suspension of 1.0 g of 5-benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid in 30 ml of dry benzene was added 0.29 ml of thionyl chloride and 0.03 ml of dimethylformamide. The mixture was left for 18 hours at room temperature and then evaporated under vacuum. To the residue so obtained were added 30 ml of ether, 1 ml of thioglycolic acid, and 1 ml of triethylamine. After 24 hours at room temperature, the reaction mixture was added to ethyl acetate, and the resultant solutions was washed with water, dried and evaporated. The residue so obtained was chromatographed on silica gel, eluting with 100:100:2 hexane:ethyl acetate:acetic acid, so as to obtain the desired product as a gum. This material was dissolved in 25 ml of ethyl acetate, and to the resulting solution was added a solution of 1.5 molar equivalents of sodium 2-ethylhexanoate in 20 ml of ethyl acetate. The sodium salt of the desired product precipitated out and was filtered, washed with ethyl acetate and dried under vacuum. The product has a decomposition point of 170°-180° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04397862
출처 데이터셋uspto-grants-1983_08
ORD IDord-3d90c9219f2f45b4aa0828f0ebcd286d
출처 메모uspto-grants-1983_08