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HRID 13941作成日:2026年10月26日

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

https://huagongshe.com/reaction/13941

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl p-toluenesulfonateHCID 6645—
反応物Benzyl chloroformateHCID 10387—
反応物DiisopropylethylamineHCID 81531—
反応物(+/-)-(5-Chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methylamineHCID 11436234—
生成物(+/-)-Benzyl (5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methylcarbamateHCID 8659855589%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728155B2
出典データセットuspto-grants-2010_06
ORD IDord-92529086747c42debf7858c6e4eac049
出典メモuspto-grants-2010_06