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HRID 855280作成日:2026年10月23日

Carbon Dioxide → 5-methyl-1H-indole-7-carboxylic acid

https://huagongshe.com/ja/reaction/855280

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物WaterHCID 962—
反応物7-Bromo-5-methyl-1H-indoleHCID 3403330—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物5-methyl-1H-indole-7-carboxylic acidHCID 6686836156%

反応条件

温度2.5 °C

反応手順

1.68 g of 7-bromo-5-methyl-indole (8 mmol) were dissolved in 30 ml THF and 15 ml of a 1.6 molar solution of n-BuLi in hexane were added at −78° C. The reaction mixture was then allowed to warm to 0-5° C. and was stirred at this temperature for 30 min. Then it was cooled again to −78° C., dry ice was added and the mixture was allowed to warm to rt. After 15 min at rt it was poured into water and extracted twice with ether. The aqueous phase was then acidified with 1 N HCl solution and extracted several times with DCM. The combined DCM extracts were then washed with brine, dried with magnesium sulfate, filtered and the solvent was evaporated. The remaining residue was triturated with n-hexane. Final filtration yielded 0.78 g (56%) of 5-methyl-1H-indole-7-carboxylic acid as light brown solid. 1H NMR (DMSO-d, 300 MHz): δ 2.41 (s, 3H), 6.44 (m, 1H), 7.31 (m, 1H), 7.58 (s, 1H), 7.61 (s, 1H), 10.91 (br s, 1H), 12.92 (br s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07259183B2
出典データセットuspto-grants-2007_08
ORD IDord-5721f061e67e4ef3ada7bb121c21c9a0
出典メモuspto-grants-2007_08