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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13930생성일: 2026년 10월 25일

Methyl p-toluenesulfonate → (+/-)-Benzyl 2,3-dihydronaphtho[1,2-b]furan-2-ylmethylcarbamate

https://huagongshe.com/reaction/13930

반응식

참여 물질

역할이름HCID투입량
반응물Methyl p-toluenesulfonateHCID 6645—
반응물Benzyl chloroformateHCID 10387—
반응물DiisopropylethylamineHCID 81531—
반응물(+/-)-1-(2,3-Dihydronaphtho[1,2-b]furan-2-yl)methanamineHCID 11390012—
생성물(+/-)-Benzyl 2,3-dihydronaphtho[1,2-b]furan-2-ylmethylcarbamateHCID 6953489090.4%

반응 단계

Treatment of (±)-1-(2,3-dihydronaphtho[1,2-b]furan-2-yl)methanamine (1.19 g, 5.97 mmol) with diisopropylethylamine (0.849 g, 6.57 mmol) followed by benzyl chloroformate (1.07 g, 6.27 mmol) generally according to the procedure described for Intermediate 7 afforded 1.80 g (90%) of (±)-benzyl 2,3-dihydronaphtho[1,2-b]furan-2-ylmethylcarbamate as a white solid. Rf=0.47 (silica, ethyl acetate:hexanes 1:4); mp 110-112° C.; Anal. calcd. for C21H19NO3: C, 75.66; H, 5.74; N, 4.2. Found: C, 75.4; H, 5.57; N, 4.12. Chiral HPLC separation of (±)-benzyl 2,3-dihydronaphtho[1,2-b]furan-2-ylmethylcarbamate (Chiralcel OJ, ethanol) provided two fractions. Fraction 1 (Rt=19.572 min, Chiralcel OJ, ethanol); Fraction 2 (Rt=30.782 min, Chiralcel OJ, ethanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728155B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-8fd14a0d79cd471bbbed75be34ed846e
출처 메모uspto-grants-2010_06