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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 630690생성일: 2026년 10월 26일

Triethylamine → (1R,4S)-4-Amino-1,2,3,4-tetrahydronaphthalen-1-ol

https://huagongshe.com/reaction/630690

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl trifluoroacetateHCID 9794—
반응물1-Aminotetralin, (S)-HCID 7058074—
용매MethanolHCID 887—
생성물(1R,4S)-4-Amino-1,2,3,4-tetrahydronaphthalen-1-olHCID 8668667499.4%

반응 단계

Ethyl trifluoroacetate (24.2 mL, 204 mmol) was added dropwise to a solution of (S)-(1,2,3,4-tetrahydro-naphthalen-1-yl)amine (Alfa Aesar; 25.0 g, 170 mmol) and triethylamine (35.5 mL, 255 mmol) in MeOH (250 mL) at RT and stirred for 18 h. The mixture was concentrated to approximately ⅓ of its volume and then partitioned between DCM (200 mL) and water (200 mL). The aqueous layer was extracted into DCM (3×) and the combined organic layers were washed with brine, dried (MgSO4) and concentrated in vacuo to yield the title compound (41.1 g, 169 mmol, 99%). 1H NMR (400 MHz, CDCl3): 1.80-1.95 (3H, m), 2.05-2.15 (1H, m), 2.75-2.90 (2H, m), 5.18-5.25 (1H, q, J 5.0 Hz), 6.38-6.48 (1H, br s), 7.12-7.16 (1H, m), 7.20-7.26 (3H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315503B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-a263df2780b2487f89fffcfa1fd5d381
출처 메모uspto-grants-2016_04