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HRID 434532作成日:2026年10月26日

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

https://huagongshe.com/reaction/434532

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物Thioglycolic AcidHCID 1133—
反応物KetorolacHCID 3826—
反応物DimethylformamideHCID 6228—
反応物Thionyl ChlorideHCID 24386—
溶媒Diethyl EtherHCID 3283—
溶媒TriethylamineHCID 8471—
溶媒Ethyl AcetateHCID 8857—
生成物Carboxymethyl Benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-thiocarboxylateHCID 53956230—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04397862
出典データセットuspto-grants-1983_08
ORD IDord-3d90c9219f2f45b4aa0828f0ebcd286d
出典メモuspto-grants-1983_08