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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8726생성일: 2026년 10월 24일

Water → 1,1-Dimethylethyl 3,4-dihydro-5-(hydroxymethyl)-2(1H)-isoquinolinecarboxylate

https://huagongshe.com/ko/reaction/8726

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ammonium ChlorideHCID 25517—
반응물Sodium borohydrideHCID 4311764—
반응물Tert-butyl 5-formyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylateHCID 22335239—
용매MeOH tetrahydrofuranHCID 21899815—
생성물1,1-Dimethylethyl 3,4-dihydro-5-(hydroxymethyl)-2(1H)-isoquinolinecarboxylateHCID 6956121668.8%

반응 단계

To solution of 5-formyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester 20a (0.44 g, 1.71 mmol) in 40 mL of methanol:tetrahydrofuran (1:1) at room temperature was added sodium borohydride (0.072 g, 1.88 mmol), and the mixture was stirred to room temperature for 3 h. Water (30 mL) was added followed by ammonium chloride saturated solution (20 mL) and the product was extracted with dichloromethane. The combined organics were dried over magnesium sulfate, the solvent was evaporated and the residue was purified by flash chromatography eluting with 30% ethyl acetate in hexanes, to yield 0.31 g of 5-hydroxymethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester 21a.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091200B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b8ea807d82c04522b1c9cb4cd3a35d20
출처 메모uspto-grants-2006_08