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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1770766생성일: 2026년 10월 27일

Formaldehyde → 3,5-Dimethyl-5-nitro-1,3-oxazinane

https://huagongshe.com/reaction/1770766

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물MethylamineHCID 6329—
반응물2-Methyl-2-nitro-1,3-propanediolHCID 6480—
생성물3,5-Dimethyl-5-nitro-1,3-oxazinaneHCID 20183063.6%

반응 단계

To a solution of 2-nitro-2-methyl-1,3-propanediol (20.4 g, 151 mmol) in 40% aqueous methylamine (11.7 g, 151 mmol), was added an aqueous solution of formaldehyde (37% formaldehyde, 12.2 g, 151 mmol). The reaction was stirred at room temperature for one week, then extracted with ether three times. The organic fractions were dried over sodium sulfate and concentrated under reduced pressure to give a crude oil which was purified by column chromatography (50 to 100% ethyl acetate in hexanes) to give the desired product (15.4 g, 96.1 mmol, 63%). 1H NMR (400 MHz, CDCl3) δ 1.45 (s, 3H), 2.32 (s, 3H), 2.63-2.66 (d, J=13.2 Hz, 1H), 3.51-3.54 (d, J=12.6 Hz, 1H), 3.67-3.71 (dt, J=1.9, 13.2 Hz, 1H), 3.86-3.89 (d, J=8.5 Hz, 1H), 4.29-4.32 (dd, J=1.2, 8.6 Hz, 1H), 4.61-4.66 (dd, J=2.4, 12.6 Hz, 1H). 13C NMR (100 MHz, CDCl3) δ 22.0, 39.9, 59.8, 71.2, 83.1, 86.1. LRMS (ESI/APCI) m/z 161 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09248117B2
출처 데이터셋uspto-grants-2016_02
ORD IDord-763f22c6f1194c498805a7445679fcc6
출처 메모uspto-grants-2016_02