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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74763생성일: 2026년 10월 25일

9-Fluorenylmethyl chloroformate → 3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylpropanoic acid

https://huagongshe.com/reaction/74763

반응식

참여 물질

역할이름HCID투입량
반응물9-Fluorenylmethyl chloroformateHCID 34367—
반응물DiisopropylethylamineHCID 81531—
반응물3-Amino-2,2-dimethylpropanoic acid hydrochlorideHCID 53407724—
용매DichloromethaneHCID 6344—
생성물3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylpropanoic acidHCID 4502443145.2%

반응 단계

To 3-amino-2,2-dimethylpropanoic acid, hydrochloride salt (250 mg, 1.63 mmol, 1 eq.) in dichloromethane (4 mL, 0.4 M) was added diisopropylethylamine (859 μL, 4.88 mmol, 3 eq.) followed by (9H-fluoren-9-ylmethoxy)carbonyl chloride (473 mg, 1.79 mmol, 1.1 eq.) The reaction was stirred for 18 hours and then concentrated in vacuo. The residue was taken up in ethyl acetate (3 mL) and washed with 1 M aqueous hydrochloric acid solution (2×1 mL) and with brine. The organic layer was dried over sodium sulfate, filtered, and purified by silica gel chromatography (Gradient: 0% to 100% ethyl acetate in heptane) to give #93 (250 mg, 45%) as an oil. 1H NMR (400 MHz, DMSO-d6) δ 12.22 (s, 1H), 7.89 (d, J=7.4 Hz, 2H), 7.72 (d, J=7.4 Hz, 2H), 7.38-7.44 (m, 2H), 7.27-7.35 (m, 3H), 4.18-4.30 (m, 3H), 3.16 (d, J=6.2 Hz, 2H), 1.05 (s, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828401B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e69ad027905349daab7a1ad374bc14e2
출처 메모uspto-grants-2014_09