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HRID 583779생성일: 2026년 10월 25일

3-Acetylindole → tert-Butyl 3-acetyl-1H-indole-1-carboxylate

https://huagongshe.com/reaction/583779

반응식

참여 물질

역할이름HCID투입량
반응물3-AcetylindoleHCID 12802—
반응물Di-tert-butyl dicarbonateHCID 90495—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl 3-acetyl-1H-indole-1-carboxylateHCID 14593498—

반응 단계

To a stirred solution of 3-acetylindole (0.01 mol) in THF is added (BOC)2O (0.01 mol) and a tertiary amine base (0.01 mol), and the mixture is stirred. Reaction progress may be followed by TLC or HPLC. When a sufficient amount of desired product is formed, the mixture (or, optionally, the residue which is obtained after first rotary evaporating off the reaction solvent) is partitioned between ethyl acetate and an excess of about 0.1 M sodium hydroxide. The organic layer is washed with brine, dried over sodium sulfate, and rotary evaporated to give 3-acetyl-1-(tert-butoxycarbonyl)-indole, which may be purified, if needed or desired, by chromatography on silica gel or crystallization.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06924276B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-03702e6931274fa9b08f397e5b399321
출처 메모uspto-grants-2005_08