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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13941생성일: 2026년 10월 25일

Methyl p-toluenesulfonate → (+/-)-Benzyl (5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methylcarbamate

https://huagongshe.com/reaction/13941

반응식

참여 물질

역할이름HCID투입량
반응물Methyl p-toluenesulfonateHCID 6645—
반응물Benzyl chloroformateHCID 10387—
반응물DiisopropylethylamineHCID 81531—
반응물(+/-)-(5-Chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methylamineHCID 11436234—
생성물(+/-)-Benzyl (5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methylcarbamateHCID 8659855589%

반응 단계

Treatment of (±)-1-(5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methanamine (0.83 g, 3.07 mmol) with diisopropylethylamine (1.20 g, 9.28 mmol) followed by benzyl chloroformate (0.79 g, 4.60 mmol) generally according to the procedure described for Intermediate 7 provided 1.00 g (89%) of (±)-benzyl (5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methylcarbamate as a white solid. mp 117-119° C.; Anal. calcd. for C21H18ClNO3.0.5H2O: C, 66.93; H, 5.08; N, 3.72. Found: C, 66.81; H, 4.96; N, 3.67.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728155B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-92529086747c42debf7858c6e4eac049
출처 메모uspto-grants-2010_06