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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39269생성일: 2026년 10월 23일

Hydrochloric Acid → O-(4,4-bis(diethylphosphoryl)butyl)-L-tyrosine

https://huagongshe.com/ko/reaction/39269

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물N-(9-fluorenylmethoxycarbonyl)-O-(4,4-bis(diethylphosphoryl)butyl)-L-tyrosineHCID 86762026—
용매WaterHCID 962—
용매piperidine N,N-dimethylformamideHCID 23501187—
생성물O-(4,4-bis(diethylphosphoryl)butyl)-L-tyrosineHCID 8676202597.8%

반응 단계

A solution of 84 (490 mg, 0.622 mmol) in piperidine/DMF (1:1, 4 mL) was stirred at room temperature for 45 min. After diluting with water and adjusting the pH to ˜3 by the addition of 1N HCl the aqueous layer was washed with diethyl ether (2×) then the pH was readjusted to ˜10 by the addition of 1N NaOH. The product was extracted with ethyl acetate (3×) washed with saturated aqueous NaCl and dried over Na2SO4. The crude material was purified by silica gel chromatography (0 to 10% methanol in CH2Cl2 over 10 column volumes then 10 to 20% over 5 column volumes) using a Biotage Horizon™ apparatus resulting in the colourless liquid 85 (271 mg, 77%): 1H NMR (400 MHz, CDCl3) δ 1.33 (t, J=7.1, 6H), 1.34 (t, J=7.1, 6H), 1.43 (s, 9H), 2.04-2.17 (m, 4H), 2.37 (tt, J=5.8, 24.1, 1H), 2.77 (dd, J=7.6, 13.7, 1H), 2.97 (dd, J=5.5, 13.7, 1H), 3.55 (dd, J=5.5, 7.6, 1H), 3.94 (t, J=5.8, 2H), 4.14-4.23 (m, 8H), 6.78 (d, J=8.6, 2H), 7.10 (d, J=8.6, 2H): 31P (162 MHz, CDCl3) δ 24.76 (s, 2P).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524691B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-e455a51751ba446b913ba39770484f9f
출처 메모uspto-grants-2013_09