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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1291776생성일: 2026년 10월 25일

Triethylamine → N-methoxyethoxyacetyl-(L)-valine tert-butyl ester

https://huagongshe.com/reaction/1291776

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(2-Methoxyethoxy)acetic acidHCID 27642—
반응물Diethyl cyanophosphonateHCID 76257—
반응물tert-Butyl L-valinateHCID 114626—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N-methoxyethoxyacetyl-(L)-valine tert-butyl esterHCID 8070703281.2%

반응 단계

At 0°, 6.4 ml (45.7 mmol) of triethylamine are added to a solution of 5 g (23.9 mmol) of (L)-valine tert-butyl ester, 2.91 g (21.7 mmol) of 2-(methoxyethoxy)-acetic acid and 3.55 g (21.7 mmol) of cyanophosphonic acid diethyl ester in 30 ml of DMF and the mixture is then stirred overnight at RT. The reaction mixture is diluted with methylene chloride, washed in succession with 10% citric acid, saturated sodium hydrogen carbonate solution and saturated sodium chloride solution and, after concentration by evaporation of the organic phase, yields 5.1 g of N-methoxyethoxyacetyl-(L)-valine tert-butyl ester, which is stirred for 1 h at RT in 22 ml of a (1:1) mixture of methylene chloride and TFA. Concentration by evaporation of the reaction solution yields the title compound in the form of a colourless oil. 1H-NMR (200 MHz, CDCl3): 10.0 (s, broad, 1H), 7.62 d, broad, 1H), 4.55 (m, 1H), 4.10 (s, 2H), 3.70 (m, 2H), 3.58 (m, 2H), 3.40 (s, 3H), 2.28 (m, 1H), 0.98 (d, J=7 Hz, 3H), 0.95 (d, J=7 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05753652
출처 데이터셋uspto-grants-1998_05
ORD IDord-6319baa8aaeb4eb9aab4cda2aff0c823
출처 메모uspto-grants-1998_05