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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1805949생성일: 2026년 10월 25일

Glycine tert-butyl ester → Tert-butyl 2-(2,2-dimethylchroman-6-sulfonamido)acetate

https://huagongshe.com/reaction/1805949

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참여 물질

역할이름HCID투입량
반응물Glycine tert-butyl esterHCID 151417—
반응물2,2-Dimethyl-6-Chromanesulfonyl ChlorideHCID 2779774—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 2-(2,2-dimethylchroman-6-sulfonamido)acetateHCID 5840909488%

반응 조건

온도25 °C

반응 단계

To the solution of 2,2-dimethylchroman-6-sulfonyl chloride (3.165 g, 10.92 mmol) in DCM (50 mL) at −30° C. was added tert-butyl 2-aminoacetate (2.308 mL, 16.39 mmol), Hunig'sBase (3.82 mL, 21.85 mmol), and catalytic amount of DMAP. The mixture was stirred at 25° C. overnight while the reddish orange color of the reaction mixture turned bright yellow. The crude reaction mixture was diluted with EtOAc, washed with dilute aqueous hydrochloric acid solution, then aqueous NaHCO3 solution and brine. The organic layer was dried over MgSO4 and removed on a rotavapor to give a creamy powder. The crude material was purified by silica chromatography (15-30% EtOAc/Hexanes) to yield 3.6 grams of an off white powder (88%). 1H NMR (500 MHz, CDCl3) δ 7.58 (d, J=2.1 Hz, 1H), 7.55 (dd, J=8.6, 2.3 Hz, 1H), 6.81 (t, J=10.6 Hz, 1H), 4.90 (s, 1H), 3.64 (d, J=5.1 Hz, 2H), 2.81 (t, J=6.7 Hz, 2H), 1.81 (t, J=6.7 Hz, 2H), 1.35 (s, 9H), 1.34 (s, 6H). LRMS [ESI, (M−H)−] m/z calcd for C17H24NO5S 354.14, found 354.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354548B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-af38c9975eda47a49ab16f97631878bd
출처 메모uspto-grants-2013_01