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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50547생성일: 2026년 10월 24일

Diethyl Ether → 3-(1-propenyl)-1,5-dihydro-3H-2,4-benzodioxepine

https://huagongshe.com/ko/reaction/50547

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물1,2-DimethoxyethaneHCID 8071—
반응물1,5-Dihydro-3-methoxy-2,4-benzodioxepinHCID 3795208—
생성물3-(1-propenyl)-1,5-dihydro-3H-2,4-benzodioxepineHCID 53720123—

반응 단계

Crude 3-methoxy-1,5-dihydro-3H-2,4 benzodioxepine (361 mg, 2.2 mmol) was dissolved in dry DME (2 mL) p-toluenesulfonic acid (95.2 mg, 0.5 mmol) and chrotonaldehyde (0.166 mL, 2 mmol) were added. The mixture was stirred at rt. for 2 h. Ether (10 mL) was added and the organic layer washed with a saturated solution of NaHCO3 and water, then dried (Na2SO2). After removed the solvent the crude was purified by cc using AcOEt/Hexane (1:1) as eluent. 3-(1-Propenyl)-1,5-dihydro-3H-2,4-benzodioxepine 3 was obtained as an oil (175 mg, 46%). 1HNMR (CDCl3): δ 7.39-7.12 (m, 4H), 5.98 (dqd, J=15.5, 6.5 and 1.0 Hz, 1H), 5.53 (ddq, J=15.5, 4.7 and 1.4 Hz, 1H), 5.32 (dd, J=4.6 and 0.8 Hz, 1H), 4.94 (d, J=14.2 Hz, 2H), 4.86 (d, J=14.2 Hz, 2H), 1.74 (dqd, J=6.4, 1.5 and 0.8 Hz, h.). 13CNMR(CDCl3): δ 5 138.8, 130.1, 127.8, 127.1, 127.0, 104.7, 70.0, 17.6.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713287B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-3a1e959f60a0497e937d008869535ae3
출처 메모uspto-grants-2004_03