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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 9-Fluorenylmethyl chloroformate | HCID 34367 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 3-Amino-2,2-dimethylpropanoic acid hydrochloride | HCID 53407724 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylpropanoic acid | HCID 45024431 | 45.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08828401B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-e69ad027905349daab7a1ad374bc14e2 |
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| 출처 메모 | uspto-grants-2014_09 |
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