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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2425329생성일: 2026년 10월 25일

Triethylamine → tert-butyl 6-bromo-3-formyl-1H-indole-1-carboxylate

https://huagongshe.com/reaction/2425329

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물6-Bromoindole-3-carbaldehydeHCID 2794830—
반응물Tert-butyl ChloroformateHCID 9920397—
용매DichloromethaneHCID 6344—
생성물tert-butyl 6-bromo-3-formyl-1H-indole-1-carboxylateHCID 11313330—

반응 조건

온도0 °C

반응 단계

6-Bromoindole-3-carboxaldehyde, 23 (5.0 g, 22.3 mmol) is dissolved in methylene chloride (40 mL), then cooled to 0° C. and tert-butylchloroformate (3.40 g, 25.0 mmol) and triethyl amine (2.50 g, 25.0 mmol) are added over 5 minutes. The reaction is maintained at reflux, under inert atmosphere for 3 hours. The reaction is cooled, filtered and the solvent removed in vacuo. The residue composed primarily of compound 24 is used in the Example 18 without purification. (See, e.g., G. Wille and W. Steglich, Synthesis, 2001, 759-762 for a related procedure.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07964649B2
출처 데이터셋uspto-grants-2011_06
ORD IDord-69c6fc11f5f84bed94d17a7a0a8b8255
출처 메모uspto-grants-2011_06