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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 708562생성일: 2026년 10월 24일

Formaldehyde → (3S)-6,7-Dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

https://huagongshe.com/ko/reaction/708562

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Sulfuric AcidHCID 1118—
반응물LevodopaHCID 6047—
용매WaterHCID 962—
생성물(3S)-6,7-Dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 12926159—

반응 단계

(S)-2-Amino-3-(3,4-dihydroxy-phenyl)-propionic acid (90 g) was suspended in 0.8 L water, then 18.2 mL concentrated sulfuric acid in 0.5 L additional water was added with stirring. Formaldehyde solution (136 mL, 37 wt %) was then added while stirring and the mixture was stirred 18 hours at rt. It was quenched by addition of 24.4 g NaOH in 0.5 L water, dropwise over 1 h while cooling. The resulting mixture was stored overnight at 4° C., and the solid that formed was collected by filtration, washed with hot water (70° C.), cooled again and collected by filtration. The solid was treated with 0.5 L MeOH and evaporated, then stored under vacuum overnight to give 65 g desired product. 1H NMR (400 MHz, MeOH-d4): 6.64 (s, 1H), 6.59 (s, 1H), 4.29-4.21 (m, 3H), 3.29-3.21 (m, 1H), 3.11-3.01 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09175003B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-ee49fe4eb61a4cb39aa4e469a5c56fb7
출처 메모uspto-grants-2015_11