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HRID 558081作成日:2026年10月27日

Hydrochloric Acid → HCID 66999647、化合物

https://huagongshe.com/reaction/558081

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TetrahydrofuranHCID 8028—
反応物trans-1-Methoxy-3-trimethylsilyloxy-1,3-butadieneHCID 5366448—
反応物7-Bromo-1-methyldibenz[b,f][1,4]oxazepineHCID 66999466—
触媒Ytterbium triflateHCID 2733225—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 66999647HCID 6699964782%

反応手順

To a solution of 7-bromo-1-methyldibenz[b,f][1,4]oxazepine (25.05 g, 86.98 mmol) and Ytterbium(III) triflate (2.8 g, 4.5 mmol) in toluene (0.21 L) at 0° C., (E)-1-methoxy-3-trimethylsilyloxy-1,3-butadiene (18 mL, 95.7 mmol) was added dropwise. THF (0.1 L) was added to dissolve the formed precipitate and the solution was stirred for 15 min. 1N hydrochloric acid (50 mL) was added and the resulting mixture was stirred for an additional 15 min, after which it was diluted with ethyl acetate and washed with brine. After drying (Na2SO4) the solvent was evaporated under reduced pressure to yield the crude compound which was triturated in methanol to give the title compound (25.4 g, 82%). Data: 1H-NMR (400 MHz, CDCl3) δ 2.31 (s, 3H), 2.43 (m, 1H), 3.00 (m, 1H), 5.23 (m, 1H), 5.41 (m, 1H), 6.99-7.52 (m, 7H). (m/z)=356+358 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063037B2
出典データセットuspto-grants-2011_11
ORD IDord-d93366eab9da4935821bb2614a02f727
出典メモuspto-grants-2011_11