돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1056819생성일: 2026년 10월 25일

Hydrochloric Acid → HCID 86713217, 화합물

https://huagongshe.com/reaction/1056819

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PiperidineHCID 8082—
반응물Triisopropyl borateHCID 21531—
반응물Sodium BicarbonateHCID 516892—
반응물4-(Pyridin-2-ylmethoxy)benzaldehydeHCID 759667—
반응물Boron monoxideHCID 6327189—
반응물HCID 86713218HCID 86713218—
용매Ethyl AcetateHCID 8857—
용매Sodium chloride; waterHCID 57417360—
생성물HCID 86713217HCID 8671321745%

반응 조건

온도70 °C

반응 단계

In a 20 mL reaction vessel were placed 31.0 mg (136 μmol) of 6-(1H-indol-3-yl)hex-5-ene-2,4-dione and 13.2 mg (0.190 mmol) of boron oxide and they were dissolved in 0.88 mL of ethyl acetate. To the mixture under stirring at 70° C., 29 mg (0.14 mmol) of 4-(2-pyridylmethoxy)benzaldehyde and 62 μL (0.27 mmol) of triisopropyl borate were sequentially added. After the mixture was stirred at the same temperature for 1 hour, a solution of 2.7 μL (27 μmol) of piperidine in ethyl acetate (0.135 mL) was added and the mixture was further stirred for 1 hour. To the reaction mixture was added a 1:1 solution (0.4 mL) of 1 N hydrochloric acid and saturated brine at room temperature and the mixture was stirred for 5 minutes to 1 hour (further, the mixture was neutralized with a saturated sodium bicarbonate aqueous solution as needed). The resulting organic phase was directly subjected to purification by silica gel column chromatography (hexane/ethyl acetate or methylene chloride/methanol) to give 25.7 mg (45% yield) of the title compound as an orange powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09399635B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-92ca296526514b4f828e0c350bd1f3a9
출처 메모uspto-grants-2016_07