Sodium Hydroxide → HCID 12897089, 화합물

Methyl 5-chloropyrrole-3-carboxylate (900 g.) was refluxed for 9 hours with 20 ml. of methanol and 10 ml. of 1 N sodium hydroxide. Methanol was removed by evaporation, the aqueous residue was diluted with approximately 10 ml. of water and extracted twice with ether. The aqueous phase was acidified with conc. hydrochloric acid and product extracted into ethyl acetate. The three ethyl acetate extracts were combined, washed with saturated sodium chloride, dried over anhydrous sodium sulfate and evaporated to product (715 mg., m.p. 175°-178° C.). Recrystallization from methylene chloride/hexane afforded purified 5-chloropyrrole-3-carboxylic acid (300 mg., m.p. 178°-180° C.).

1. customMethanol was removed by evaporation
2. additionthe aqueous residue was diluted with approximately 10 ml
3. extractionof water and extracted twice with ether
4. extractionextracted into ethyl acetate
5. washwashed with saturated sodium chloride
6. dry with materialdried over anhydrous sodium sulfate
7. customevaporated to product (715 mg., m.p. 175°-178° C.)
8. customRecrystallization from methylene chloride/hexane
9. customafforded
10. custompurified 5-chloropyrrole-3-carboxylic acid (300 mg., m.p. 178°-180° C.)

ORD 기록

ord-abf783cf45ed4cfb91089997183a543c

출처 데이터셋

uspto-grants-1982_09

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US04351843