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HRID 47099作成日:2026年10月25日

2,5-Hexanedione → 3-Sulphamoyl-4-phenoxy-5-[beta-(2,5-dimethyl-1-pyrrolyl)-ethyl]-benzoic acid

https://huagongshe.com/reaction/47099

反応式

関与物質

役割名称HCID仕込み量
反応物2,5-HexanedioneHCID 8035—
反応物AluminumHCID 5359268—
反応物3-Sulphamoyl-4-phenoxy-5-[beta-aminoethyl]-benzoic acidHCID 12795717—
溶媒HexamethylphosphoramideHCID 12679—
生成物3-Sulphamoyl-4-phenoxy-5-[beta-(2,5-dimethyl-1-pyrrolyl)-ethyl]-benzoic acidHCID 13021084—

反応手順

A mixture of 3-sulphamoyl-4-phenoxy-5-[β-aminoethyl]-benzoic acid (5.0 g=1.35 mmols; see Example 3 for the preparation), acetonylacetone (1.85 g, approximately 16.2 mmols) and hexamethylphosphoric acid triamide (Hexametapol; 25 ml) is warmed at 100° for 30 minutes under N2 in an apparatus which has been protected against incident light by covering it with aluminium foil, and the reaction solution is worked up as follows, with strict exclusion of light throughout: pouring into ice-water (50 ml) and extracting with ethyl acetate, washing the extract with water, drying and filtering and evaporating the filtrate. The crude product is recrystallised from chloroform/cyclohexane with the addition of active charcoal and gives pale orange-coloured, light-sensitive crystals, melting point>210° (decomposition).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04176190
出典データセットuspto-grants-1979_11
ORD IDord-970005fb4a7e42419affa6245d0b5231
出典メモuspto-grants-1979_11