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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1285586생성일: 2026년 10월 26일

Benzene → 5-Methyl-5-nitro-1,3-dioxane

https://huagongshe.com/reaction/1285586

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물p-Toluenesulfonic acidHCID 6101—
반응물2-Methyl-2-nitro-1,3-propanediolHCID 6480—
반응물CID 19593658HCID 19593658—
용매Benzene--water (1/1)HCID 22272175—
생성물5-Methyl-5-nitro-1,3-dioxaneHCID 14518—

반응 단계

2-Nitro-2-methyl-1,3-propanediol 405.00 grams (3.00 moles), 98% trioxane 92.80 grams (1.00 mole), p-toluenesulfonic acid 3.00 grams (0.016 mole), and benzene 600 ml were placed in a two liter three-necked RB flask. The flask was fitted with a thermometer, a mechanical stirrer and a Dean-Stark trap connected to a condenser. The mixture was stirred and refluxed. The slurry gradually became a homogeneous solution (usually about 30 minutes after heating started) and the benzene-water azeotrope started to distill over. Refluxing was continued until 45 ml of water was collected (i.e., approximately four hours). During this period the solution temperature was between 78° C. and 82° C. After 45 ml of water had been collected, the reaction mixture was cooled and neutralized with 3 ml triethylamine. Benzene was distilled from the clear solution first at atmospheric pressure (approximately 415 ml benzene was recovered at a solution temperature of 82° C.-100° C.) and then at about 125 mm of pressure (approximately 120 ml benzene was recovered at a solution temperature of about 48° C.-110° C.). A clear, pale-yellow, viscous liquid, 450.67 grams, containing a mixture of the reaction products polynitroformal and 5-methyl-5-nitro-1,3-dioxane was obtained as the resulting product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04567302
출처 데이터셋uspto-grants-1986_01
ORD IDord-bfccfeef9e32469295b1c3f19408cf81
출처 메모uspto-grants-1986_01